03 Equip and Lighting Mounting.pdf

RETURN OF SUBMITTAL

Title Or Description Date: Spec. Section:

Chris Bantner 13611 East Colfax Ave.

Aurora, CO 80045

Kiewit-Turner. a Joint Venture

Contract No:

Project No:

13611 East Colfax Avenue

VA1 01 F-i 5-0-0005

554-501 Aurora, CO 80045 Transmittal Date:

VA File No:

9/29/2015

26 55 71 - 001 - R4

Submittal Scope 26 55 71 Medical Booms & Lights Resubmittal of all information up to and including JSI 118.3, the final design deferred area. This includes:

SECTION A - LEVEL 1 - ISO / EXAM PROCEDURE - DAT BUILDING 3

SECTION B - LEVEL 2 - RECOVERY - DAT BUILDING 3

SECTION C - LEVEL 3 - MINOR PROCEDURE - DAT BUILDING 3

SECTION D - LEVEL 3 - EGD COLONOSCOPY - DAT BUILDING 3

SECTION E - LEVEL 3 - BRONCHOSCOPY - DAT BUILDING 3

SECTION F - LEVEL 3 - GENERAL OR - DAT BUILDING 3

SECTION G - LEVEL 3 - CVOR - DAT BUILDING 3

SECTION H - LEVEL 3 - OR 3 - NEURO - DAT BUILDING 3

SECTION I - LEVEL 3 - OR 4 - ORTHO - DAT BUILDING 3

SECTION J - LEVEL 3-OR 5- DAVINCI - CYSTO - DAT BUILDING 3

SECTION K - CYSTOSCOPY - BUILDING 5 IBN

SECTION L - PROCEDURE - BUILDING 9 - CBC

SECTION M - GENERAL DRAWINGS

SECTION N - LEVEL 3 DAT - HYBRID CVOR

SECTION 0 - LEVEL 3 DAT - PROCEDURE

SECTION P - LEVEL 3 DAT - OATH LAB

SECTION 0 - BUILDING 4 LEVEL RCP - AUTOPSY

SECTION R - UPGRADE OPTION

Submittal Items Acted Upon

Submittal Item Status

001 - Haldeman Homme 9/3/15 Letter of Clarification ANR- Approved as Noted, Resubmit

Supplier or Manufacturer Submittal Type

Haldeman Homme Letter of Affidavit

Notes/Comments [10/23/2015 U.S. Dept of Veterans Affairs - Scott Kelly]

1. Regarding the Section R 'Upgrade Option", KT is required to provide booms that meet the contract requirements, including having the capacity to route the number of utilities specified by the final design deferred area design. No utilities were revised in the design deferred spaces except JSI 118.3 rooms since submittal 2655 71 -01 R3 was returned to KT on 12/8/14. Based on this, it would appear that KT's previous submittals including 26 55 71-01 R3 were non-compliant because the submitted Amico 90 KG equipment booms were incapable of supporting the current design utilities at the time of submittal based

Received 10/26/2015

RETURN OF SUBMITTAL

VA File No: 265571-001-R4 on the Section R information. Additionally, it would appear that this submittal is non-compliant because the equipment boom drawings in both the previously submitted room sections and the additional sections for JSI 118.3 rooms do not depict the necessary Amico 200 KG equipment booms per the information provided. The previous history of these submittals with respect to equipment boom non-compliance is also referenced, previous submittal reviews have identified the lack of any specified smoke evacuation provisions (26 55 71-01), the lack of an engineered boom-mounted smoke evacuation solution (26 55 71-01 Ri and 2655 71-01R2), and the lack of vertical travel capability (26 55 71-01 Ri). Based on all of the above, this submittal has been reviewed in detail with responses to any and all noted clarifications provided, and is being returned "APPROVED AS NOTED, RESUBMIT", with the expectation that KT will provide surgical booms and lights that meet all requirements. This office is performing a detailed analysis of the surgical boom and light revisions that occurred from the original JSI 66 revision on 9/23/13, 6 months prior to the original submittal, through the final design deferred design completion to determine and document the specific revisions in the surgical boom and light design including utilities and overall number of booms and lights required. Any request for additional compensation must be formally addressed by KT in the proper manner as part of the work authorization. Refer to Item 3 below for a potential alternate solution to the equipment boom size increase.

2. It is KT's responsibility to ensure that submittals are coordinated with the current contract design. The VA's review of submittals shall not take the place of KT submittal Quality Control procedures. Detailed review comments are provided, but KT has the ultimate responsibility for compliance.

3. It is not acceptable for the smoke evacuation exhaust to be openly exhausted into the unventilated, non-plenum interstitial space. Either connect the smoke evacuation outlet to the nearest return duct above the ceiling with airtight connection provisions, or provide information from the manufacturer that exhaust provisions through the boom to evacuate the smoke remotely are not required, and the Buffalo ViroVac can be locally exhausted in the surgical space with no risk to the users. If the latter approach is confirmed, the Section R "Upgrade Option" can be revisited, removal of the Smoke E-vac exhaust hose from the boom may allow use of the Amico 90 KG equipment boom to accommodate all specified utilities.

4. The requested information regarding the camera control connector type needs to be addressed in detail in a RFI for review, it is unclear what clarification information is requested.

5. Referenced Variance Request 359 was approved on 9/23/15.

6. Refer to architectural interior elevations for locations of wall control boxes and camera control boxes.

Submit detailed RFI if clarification is required.

Submittal Item Status

002 - Surgical Boom and Light Shop Drawings ANR- Approved as Noted, Resubmit

Supplier or Manufacturer Submittal Type

Amico Shop Drawings

Notes/Comments

1. Refer to all noted comments.

2. There are numerous locations in the Amico shop drawings containing statements such as "It is the responsibility of the hospital", "It is the hospital/GC responsibility", "to be provided by the hospital", or "the hospital must provide. The complete installation of the surgical lights and booms and all provisions for such are specified under the construction contract, thus, it is Kis responsibility to provide and coordinate

OF SUBMITTAL

all such provisions.

3. There are numerous NOTES in the lower left corner of Amico Electrical Schematic Verifications that have been addressed by previous submittal comments regarding compliance with the contract and applicable codes. It is KTs responsibility to ensure that the submitted items are in compliance with all contract requirements and applicable codes.

4. The location of the ceiling grid on numerous field of motion layout drawings is noted as erroneous. It is KTs responsibility to coordinate with contract reflected ceiling plans and applicable equipment plans.

5. For all rooms utilizing isolated power circuits for the booms, circuits are clearly shown with separate home runs from the boom. Do not combine raceways where independent isolated power or critical circuit home runs are shown on contract electrical drawings.

6. There are numerous discrepancies noted for coordination of surgical boom and light manufacturer requirements with contract drawings. Submit the following two RFIs to address these discrepancies prior to any resubmittal:

a. Section K Cystoscopy - Submit RFI regarding coordination of access panel with 2'x4' light fixtures.

b. Submit RFI regarding electrical circuit coordination:

i. Section G OR 03-03-F2-01; Drawing 03.ES.413.2_JSI 118.3 shows only 2 isolated power circuits for perfusion boom receptacles, 3 are required byAmico.

ii. Section N CVOR 03-03-D2-04; Drawing 03.ES.413.2_JSI 118.3 shows receptacle symbol in lieu of junction box for 3 isolated power circuits for equipment boom receptacles.

iii. Section N CVOR 03-03-D2-04; Drawing 03.ES.413.2_JSI 118.3 shows only 2 isolated power circuits for perfusion boom receptacles, 3 are required byAmico.

iv. Section N CVOR 03-03-D2-04; Drawing 03.ES.413.2_JSI 118.3 shows a circuit fora surgical light at the anesthesia boom, no surgical light is specified at this boom.

Signature of uthorizing Official

L

Date

Fax: 303.930.9001

303.930.9000Tel:

Kiewit - Turner a Joint Venture

Suite A-300 7200 S. Alton Way

Englewood, CO 80112

Job: 15387 - Replacement Medical Center Facility

Product Data

Sample

Other

Shop Drawing

Resubmittal

First Submittal X

VA Proj #:

To: H+L Architecture 1755 Blake Street

Suite 400

Denver, CO 80202

DESCRIPTIONSpecificationSUBMITTAL

ItemQuantity Section Sub./SupplierNo. Mfgr.

ACTION

DCBA E

Kiewit Submittal No. 22 13 00-01 Architect's Submittal No. 00008

Review Cycle: 001

Attn: Chuck Adkisson

1 SWPPP - CBS & RFP #3 OnlyKiewit - Turner a

Joint Venture

01 573

ACTION TAKEN

CONTRACTOR'S SIGNATURE:

CONTRACTOR'S NOTES:

DATE: 7/12/2011

Reviewed Only for Revisions to

Reviewed: Incorporate Changes

Reviewed=

A

B

C

Previous Submittal

Revise and Resubmit=D

Rejected =E

ARCHITECT/ENGINEER RESPONSE:

REMARKS:

BY: DATE:

Expedition f_sb_pks_01a

VA101CFM-C-0100

Cc: Tim Pogany, U.S. Dept. of Veterans Affairs

Received By ___________________

Date _______________

26 55 71

X

Medical and Surgical Lighting Fixtures

X

HaldemanHomme, Inc.

26 55 7101R4

09/29/2015

10/13/2015

Kiewit-Turner Submittal No.

VA 1

JVT 2

REQUESTED RETURN DATE:

Kevin Lindsey, U.S. Dept. of Veterans Affairs

VA101F-15-C-0005

13611 E. Colfax Avenue 2nd Floor Aurora, CO 80045

By VACO BoltonT at 11:56 am, Oct 19, 2015

These shop drawings/submittals have been reviewed in accordance with the provisions of the Contract Documents. Kiewit-Turner's review shall not serve to relieve Subcontractors or Suppliers of contractual responsibilities for any error or deviation from contract and subcontract requirements.

KIEWIT-TURNER

a Joint Venture

REVIEWED - NO COMMENTS MADE

REVIEWED WITH COMMENTS

RESUBMITTAL REQUIRED

DATE SIGNED

SUBMITTAL #: 26 55 71-01R4

09/29/15 Mark S. Johnson

05 OCT 2015

26 55 71-01R4

CRA/JTB,MWJ; H+L/KA; SAM/CM

10/16/2015

X RESUBMIT

RSK

10/23/15

Submittal 26 55 71-01R4 VA Return of Submittal Comments:

Comments regarding Haldeman Homme Letter of Clarification dated 9/3/15:

1. Regarding the Section R “Upgrade Option”, KT is required to provide booms that meet the contract requirements, including having the capacity to route the number of utilities specified by the final design deferred area designs. No utilities were revised in the design deferred spaces except JSI

118.3 rooms since submittal 26 55 71-01R3 was returned to KT on 12/8/14. Based on this, it would appear that KT’s previous submittals including 26 55 71-01R3 were non-compliant because the submitted Amico 90 KG equipment booms were incapable of supporting the current design utilities at the time of submittal based on the Section R information. Additionally, it would appear that this submittal is non-compliant because the equipment boom drawings in both the previously submitted room sections and the additional sections for JSI 118.3 rooms do not depict the necessary Amico 200 KG equipment booms per the information provided. The previous history of these submittals with respect to equipment boom non-compliance is also referenced, previous submittal reviews have identified the lack of any specified smoke evacuation provisions (26 55 71-01), the lack of an engineered boom-mounted smoke evacuation solution (26 55 71-01R1 and 26 55 71-01R2), and the lack of vertical travel capability (26 55 71-01R1). Based on all of the above, this submittal has been reviewed in detail with responses to any and all noted clarifications provided, and is being returned “APPROVED AS NOTED, RESUBMIT”, with the expectation that KT will provide surgical booms and lights that meet all requirements. This office is performing a detailed analysis of the surgical boom and light revisions that occurred from the original JSI 66 revision on 9/23/13, 6 months prior to the original submittal, through the final design deferred design completion to determine and document the specific revisions in the surgical boom and light design including utilities and overall number of booms and lights required. Any request for additional compensation must be formally addressed by KT in the proper manner as part of the work authorization. Refer to Item 3 below for a potential alternate solution to the equipment boom size increase.

2. It is KT’s responsibility to ensure that submittals are coordinated with the current contract design. The VA’s review of submittals shall not take the place of KT submittal Quality Control procedures. Detailed review comments are provided, but KT has the ultimate responsibility for compliance.

3. It is not acceptable for the smoke evacuation exhaust to be openly exhausted into the unventilated, non-plenum interstitial space. Either connect the smoke evacuation outlet to the nearest return duct above the ceiling with airtight connection provisions, or provide information from the manufacturer that exhaust provisions through the boom to evacuate the smoke remotely are not required, and the boom-mounted Buffalo ViroVac can be locally exhausted in the surgical space with no risk to the users. If the latter approach is confirmed, the Section R “Upgrade Option” can be revisited, removal of the Smoke E-vac exhaust hose from the boom may allow use of the Amico 90 KG equipment boom to accommodate all specified utilities.

4. The requested information regarding the camera control connector type needs to be addressed in detail in a RFI for review, it is unclear what clarification information is requested.

5. Referenced Variance Request 359 was approved on 9/23/15.

6. Refer to architectural interior elevations for locations of wall control boxes and camera control boxes. Submit detailed RFI if clarification is required.

Shop Drawing Comments:

1. Refer to all noted comments.

2. There are numerous locations in the Amico shop drawings containing statements such as “It is the responsibility of the hospital”, “It is the hospital/GC responsibility”, “to be provided by the hospital”, or “the hospital must provide”. The complete installation of the surgical lights and booms and all provisions for such are specified under the construction contract, thus, it is KT’s responsibility to provide and coordinate all such provisions.

3. There are numerous NOTES in the lower left corner of Amico Electrical Schematic Verifications that have been addressed by previous submittal comments regarding compliance with the contract and applicable codes. It is KT’s responsibility to ensure that the submitted items are in compliance with all contract requirements and applicable codes.

4. The location of the ceiling grid on numerous field of motion layout drawings is noted as erroneous. It is KT’s responsibility to coordinate with contract reflected ceiling plans and applicable equipment plans.

5. For all rooms utilizing isolated power circuits for the booms, circuits are clearly shown with separate home runs from the boom. Do not combine raceways where independent isolated power or critical circuit home runs are shown on contract electrical drawings.

6. There are numerous discrepancies noted for coordination of surgical boom and light manufacturer requirements with contract drawings.

Submit the following two RFIs to address these discrepancies prior to resubmittal:

a. Section K Cystoscopy - Submit RFI regarding coordination of access panel with 2’x4’ light fixtures.

b. Submit RFI regarding electrical circuit coordination:

i. Section G OR 03-03-F2-01; Drawing 03.ES.413.2_JSI 118.3 shows only 2 isolated power circuits for perfusion boom receptacles, 3 are required by Amico.

ii. Section N CVOR 03-03-D2-04; Drawing 03.ES.413.2_JSI 118.3 shows receptacle symbol in lieu of junction box for 3 isolated power circuits for equipment boom receptacles.

iii. Section N CVOR 03-03-D2-04; Drawing 03.ES.413.2_JSI 118.3 shows only 2 isolated power circuits for perfusion boom receptacles, 3 are required by Amico.

iv. Section N CVOR 03-03-D2-04; Drawing 03.ES.413.2_JSI 118.3 shows a circuit for a surgical light at the anesthesia boom, no surgical light is specified at this boom.

Kiewit-Turner a Joint Venture 7200 S. Alton Way, Suite A-300, Englewood, CO 80112

Phone: 303-930-9000 FAX: 303-930-9001

Project Name:

Subcontractor Name: Submittal Date:

Contact Name: E-mail: Return By Date:

Contact Phone(s): Review Days:

Number: Name:

1.4.B SHOP DRAWINGS- ROOM LAYOUT DOCUMENTS

Medical & Surgical Lights - Inclusive of JSI 117 & 118.3 AMICO N/A Y Y Y X Field of Motion - Room Layouts AMICO N/A Y Y Y X

COMPLETE SUBMITTAL PACKAGE FOR ALL LIGHTS & BOOMS

M7470 Medical & Surgical Lights AIMCO/ LT-S-CN-P3SC N/A Y Y Y X M7475/M7480 Medical & Surgical Lights AIMCO/ LT-S-CN-P6SC N/A Y Y Y X

M7485 Medical & Surgical Lights AIMCO/ LT-S-CN-P6SC/P6SC N/A Y Y Y X M7490 Medical & Surgical Lights AIMCO/ LT-S-CN-P6SC/P3SC N/A Y Y Y X U4033 Medical Equipment Booms AIMCO/LP-L-11NN-N-E N/A Y N Y X

U4033.A Medical Equipment Booms

AIMCO/LP-L-11NN-N-E

TANDEM MOUNTED

W/VT-S-CN-MH1-26

N/A Y N Y X

U4035 Medical Equipment Booms AIMCO/LP-L-11NN-N-E N/A Y N Y X

Submittal is in Compliance Submittal is in Compliance with Variances from Specifications

SUBMITTAL INDEX & COVER SHEET Department of Veteran's Affairs Replacement Medical Center

Haldeman-Homme Inc. 09/03/15 Bill Tolley btolley@haldemanhomme.com 720-203-6034

Specification Section: 26 55 71 - 03 Medical and Surgical Lights

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Submittal Type

Submittal Item Description Manufacturer / Model

Signature Bill Tolley

Reviewed By Date

265571 Medical & Surgical Light Page 1 of 1

Design team please note that connection to the exhaust system is no longer required.

Depending on hose material, this hose may not be able to pass through the interstitial deck due to fire rating.

Electrical Sub:

Please note length limitations for conduit runs.

VA/JVT: Please indicate required connector type.

Refer to Return of Submittal comments

JSN # Room # Section Description (as per drawing) Room Type Equipment Type QTY U4035 E boom 18 EA 90 w/ 12.5"x18" C40 & 3 shelves & 1 smoke E vac & EA arm switch & NC & dual monitor (850) Bronchoscopy Equipment Boom 1 M7480 E ice30 (700) single mount w/ 1 camera ready & 1 camera adder Bronchoscopy Equipment Boom 1

JSN # Room # Section Description (as per drawing) Room Type Equipment Type QTY U4033.A F boom 11 w/ 12.5"x18" C30 & dual monitor (1000) General OR Anesthesia Boom 2 M7480 03 03 E3 02 F ice30 (850) single mount w/ 1 camera ready & 1 camera adder General OR Anesthesia Boom 2 U4035 03 03 D3 05 F boom 18 EA 90 w/ 12.5"x18" C40 & 3 shelves & 1 smoke E vac & EA arm switch & dual monitor (850) General OR Equipment Boom 4 M7475 F ice30 (700) single mount w/ 1 camera ready General OR Equipment Boom 4

JSN # Room # Section Description (as per drawing) Room Type Equipment Type QTY U4033.B G boom 11 w/ C30 & 26" dual monitor (1000) CVOR Perfusion Boom 1 U4035 G boom 18 EA 90 w/ 12.5"x18" C40 & 3 shelves & 1 smoke E vac & EA arm switch & dual monitor (850) CVOR Equipment Boom 2 M7475 G ice30 (700) single mount w/ 1 camera ready CVOR Equipment Boom 2 U4033.A G boom 11 w/ 12.5"x18" C30 & dual monitor (1000) CVOR Anesthesia Boom 1 M7480 G ice30 (850) single mount w/ 1 camera ready & 1 camera adder CVOR Anesthesia Boom 1

JSN # Room # Section Description (as per drawing) Room Type Equipment Type QTY U4033.A H boom 11 w/ 12.5"x18" C30 & dual monitor (1000) NEURO Anesthesia Boom 1 M7480 H ice30 (850) single mount w/ 1 camera ready & 1 camera adder NEURO Anesthesia Boom 1 U4035 H boom 18 EA 90 w/ 12.5"x18" C40 & 3 shelves & 1 smoke E vac & EA arm switch & dual monitor (850) NEURO Equipment Boom 2 M7475 H ice30 (700) single mount w/ 1 camera ready NEURO Equipment Boom 2

JSN # Room # Section Description (as per drawing) Room Type Equipment Type QTY U4033.A I boom 11 w/ 12.5"x18" C30 & dual monitor (1000) ORTHO Anesthesia Boom 1 M7480 I ice30 (850) single mount w/ 1 camera ready & 1 camera adder ORTHO Anesthesia Boom 1 U4035 I boom 18 EA 90 w/ 12.5"x18" C40 & 3 shelves & 1 smoke E vac & EA arm switch & dual monitor (850) ORTHO Equipment Boom 2 M7475 I ice30 (700) single mount w/ 1 camera ready ORTHO Equipment Boom 2

JSN # Room # Section Description (as per drawing) Room Type Equipment Type QTY U4033.A J boom 11 w/ 12.5"x18" C30 & dual monitor (1000) DA VINCI/CYSTOAnesthesia Boom 1 M7480 J ice30 (850) single mount w/ 1 camera ready & 1 camera adder DA VINCI/CYSTOAnesthesia Boom 1 U4035 J boom 18 EA 90 w/ 12.5"x18" C40 & 3 shelves & 1 smoke E vac & EA arm switch & dual monitor (850) DA VINCI/CYSTOEquipment Boom 2 M7475 J ice30 (700) single mount w/ 1 camera ready DA VINCI/CYSTOEquipment Boom 2

JSN # Room # Section Description (as per drawing) Room Type Equipment Type QTY U4035 N boom 18 EA 90 w/ 12.5"x18" C40 & 3 shelves & 1 smoke E vac & EA arm switch & NC & dual monitor (850) HYBRID CVOR Equipment Boom 1 M7480 N ice30 (700) single mount w/ 1 camera ready & 1 camera adder HYBRID CVOR Equipment Boom 1 U4033.B N boom 11 w/ C30 & 26" dual monitor (1000) HYBRID CVOR Perfusion Boom 1 U4033.A N boom 11 w/ 12.5"x18" C30 & 26" single monitor (700) & NC HYBRID CVOR Anesthesia Boom 1 U4507 N cath lab 28 with rad shield (1000) HYBRID CVOR CATH Lab 1 M7475 N ice30 (850) single mount w/ 1 camera ready HYBRID CVOR CATH Lab 1 U4508 N cath lab 28 HYBRID CVOR CATH Lab 1 M7475 N ice30 (1000) single mount w/ 1 camera ready HYBRID CVOR CATH Lab 1

03 03 D2 04

03 03 E10 02

03 03 F3 04

03 03 G3 02

03 03 G2 04

03 03 F2 01

Highlighted Units above changed to AMICO Spectra V series 200kg per Clarificaiton Letter

Clinical Solutions

Approved By: __________________________ (Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER September 1, 2015Update:

SUBMITTAL PACKAGESUBMITTAL PACKAGE

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Prepared For: VA DENVER

Date: November 04, 2014

Approved By: Approved By:

(Print) (Signature) mico w w w . a m i c o . c o m

Amico Clinical Solutions Corp. 85 Fulton Way, Richmond Hill, ON L4B 2N4, Canada 71 East Industry Court, Deer Park, NY 11729, USA

Tel: 905.764.0800 | Fax: 905.764.0862 www.amico.com

Table of Contents

SECTION A - LEVEL 1 - ISO / EXAM PROCEDURE - DAT BUILDING 3

SECTION B - LEVEL 2 - RECOVERY - DAT BUILDING 3

SECTION C - LEVEL 3 - MINOR PROCEDURE - DAT BUILDING 3

SECTION D - LEVEL 3 - EGD COLONOSCOPY - DAT BUILDING 3

SECTION E - LEVEL 3 - BRONCHOSCOPY - DAT BUILDING 3

SECTION F - LEVEL 3 - GENERAL OR - DAT BUILDING 3

SECTION G - LEVEL 3 - CVOR - DAT BUILDING 3

SECTION H - LEVEL 3 - OR 3 - NEURO - DAT BUILDING 3

SECTION I - LEVEL 3 - OR 4 - ORTHO - DAT BUILDING 3

SECTION J - LEVEL 3 - OR 5 - DA VINCI - CYSTO - DAT BUILDING 3

Amico Clinical Solutions Corp. 85 Fulton Way, Richmond Hill, ON L4B 2N4, Canada 71 East Industry Court, Deer Park, NY 11729, USA

Tel: 905.764.0800 | Fax: 905.764.0862 www.amico.com

Table of Contents

SECTION K - CYSTOSCOPY - BUILDING 5 IBN

SECTION L - PROCEDURE - BUILDING 9 - CBC

SECTION M - GENERAL DRAWINGS

SECTION N - LEVEL 3 DAT - HYBRID CVOR

SECTION O - LEVEL 3 DAT - PROCEDURE

SECTION P - LEVEL 3 DAT - CATH LAB

SECTION Q - BUILDING 4 LEVEL RCP - AUTOPSY

SECTION R - UPGRADE OPTION

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: July 28, 2015 Level: 03 - DAT Building 03 Rooms # MINOR PROCEDURE 03‐03‐D9‐04 | 03‐03‐D9‐05 | 03‐03‐E9‐04

Section C - Level 3 Clinical Solutions Section C - Level 3

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Approved By: Approved By:

(Print) (Signature)

Coordinate wall control back box location per contract documents.

Camera control box per RFI 7591a.

Ceiling grid does not reflect contract documents.

contract documents.

Camera control box per RFI 7591a.

Ceiling grid does contract documents.

Camera control box per RFI 7591a.

Ceiling grid does

Per previous conversation with HH/Amico, for these three specific rooms, this distance has been approved to a min of 3" due to interstitial deck conflicts with supports.

Per previous conversation with HH/Amico, for these three specific rooms, this distance has been approved to a min of 3" due to interstitial deck conflicts with supports.

See page 13 for typical comments.

Operative Documents provide no receptacle for monitor in these specific rooms.

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: July 28, 2015 Level: 03 - DAT Building 03 Rooms # EGD Colonoscopy 03‐03‐E9‐08 | 03‐03‐F9‐03 | 03‐03‐F9‐04 | 03‐03‐G9‐04

ERCP 1 03‐03‐F10‐03

SECTION D - LEVEL 3Clinical Solutions SECTION D- LEVEL 3

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Prepared For: VA DENVER

Date: November 04, 2014 Level: 03 Rooms # EGD Colonoscopy 03-03-E9-08 | 03-03-F9-03 | 03-03-F9-04 | 03-03-G9-04

ERCP 1 03-03-F10-03

Approved By: Approved By:

(Print) (Signature)

Ceiling grid not per contract

TYP: Structural plate will be inside the interstitial space for tandem mounts.

VA/JVT to confirm whether or not this hose material will be permitted to pass through interstitial deck.

TYP: Distance may increase due to interstitial deck coordination.

Reference RFI 7032. Exact distance will be submitted with modular equipment supports in 05 45 60.

Connect to nearest return duct above ceiling with airtight connection provisions, or delete remote exhaust provisions, reference Return of Submittal comments.

VA & JVT to confirm type, location, and quantities of boom utilities.

PM drop location per RFI 6735 Confirmed

JVT to confirm adequate circuitry.

VA/JVT to confirm acceptability.

Match receptacle orientation used for all 120V receptacles, typ.

Confirmed ref: RFI 6735 Sketch ES.X471

TYP: Due to interstitial deck, structural plate will be inside the interstitial space.

Brake power supply will be field located below interstitial deck and above ceiling.

boom utilities.

PM drop location per

RFI 6735

Confirmed

VA/JVT confirm this is acceptable.

JVT to confirm circuit quantity correct.

Confirmed

Match receptacle orientation used for all 120V receptacles, typ.

See sheet 32 for typical comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent isolated power circuit home runs.

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: September 1, 2015

03 - DAT Building 03 Level:

Room # 03‐03‐E10‐02 BRONCHOSCOPY

SECTION E - LEVEL 3Clinical Solutions SECTION E - LEVEL 3

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Prepared For: VA DENVER

Date: November 04, 2014 Level: 03 Room # 03-03-E10-02 BRONCHOSCOPY

Approved By: Approved By:

(Print) (Signature)

VA/JVT please provide dimension as it not indicated on

03.AI.413-H.

In E-W direction, provide equal spacing between boom mount and access panel, and access panel and 2'x4' light fixture. Align the North edge of the access panel and boom support.

Note change.

Equipment boom must be capable of providing all specified services, refer to Return of Submittal comment regarding Section R

Connect to nearest return duct above ceiling with airtight connection provisions, or delete boom utilities.PM drop location per

RFI 6735 Confirmed

JVT to confirm acceptable.

See comments on previous sheets

TYP: Due to interstitial deck, structural plate will be inside the interstitial space.

Brake power supply will be field located below interstitial deck and above ceiling.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: September 1, 2015 Level: 03 - DAT Building 03 Rooms # GENERAL OR 03‐03‐D3‐05 | 03‐03‐E3‐02

SECTION F - LEVEL 3Clinical Solutions SECTION F

R -A

/Ce 3Qvi

Prepared For: VA DENVER

Date: November 04, 2014 Level: 03 Rooms# GENERAL OR 03-03-D3-05 | 03-03-E3-02

Approved By: Approved By:

(Print) (Signature)

Wall control and camera control as per

26 55 71-01R3 - VA

RESPONSE

Access panels locations and offset dimensions incorrect.

Reference 03.AI.455 for access panel locations.

Location of back boxes for camera control and wall controls per operative

Wall control and camera control as per

26 55 71-01R3 - VA

RESPONSE

Access panels locations and offset dimensions incorrect.

Reference 03.AI.455 for access panel locations.

Location of back boxes for camera control and wall controls per operative boom utilities.

PM drop location per

JVT to confirm if

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent capable of providing all specified services, refer to Return of Submittal comment regarding Section R

Connect to nearest return duct above ceiling with airtight connection provisions, or delete boom utilities.VA/JVT: Please confirm if this is

PM location.

VA/JVT: Please advise. RFI 6735 sketch PL.X295 indicates two (2) CO2 for these booms. 26 55 71-01R3 indicates only one (1) CO2.

03.PP.103-A_JSI 118.3 corrected Flag Note 5 to indicate one (1) CO2 outlet for coordination

JVT to confirm if acceptable.

See sheet 43 for typical comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: September 1, 2015

03 - DAT Building 03 Level:

Room # 03‐03‐F2‐01 CVOR

SECTION G - LEVEL 3SECTION G - LEVEL 3

-A

L

W.

Wi tfjC

a. <t.

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Prepared For: VA DENVER

Date: November 04, 2014 Level: 03 Room # 03-03-F2-01 CVOR

Approved By: Approved By:

(Print) (Signature)

Location of back boxes for camera control and wall controls per operative documents.

Ceiling grid not per operative documents.

Reference

6/03.AI.455.

For access panels locations and offset dimensions, reference

6/03.AI.455.

7'-4 5/8"

Reference5/03.AI.455 for boom mount dimension mmatute Sticky Note Marked set by mmatute boom utilities.

PM drop location per

See sheet 32 for typical comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent

Note change.

Equipment boom must be capable of providing all specified services, refer to Return of Submittal comment regarding Section R

Connect to nearest return duct above ceiling with airtight connection provisions, or delete boom utilities.

VA/JVT: Please advise. RFI 6735 sketch PL.X296 indicates two (2) CO2 for these booms. 26 55 71-01R3 indicates only one (1) CO2.

VA/JVT: Please confirm if this is PM location.

Confirmed

03.PP.103-A_JSI 118.3 corrected Flag Note 5 to indicate one (1) comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent boom utilities.

PM drop location per comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: September 1, 2015 Level: 03 - DAT Building 03 Rooms # OPERATING ROOM 3 ‐ NEURO 03‐03‐F3‐04

SECTION H - LEVEL 3Clinical Solutions SECTION H - LEVEL 3

R -A m m

A

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Prepared For: VA DENVER Date: November 04, 2014 Level: 03 Rooms # OPERATING ROOM 3 - NEURO 03-03-F3-04

Approved By: Approved By:

(Print) (Signature) control and wall controls per operative documents

Access panel locations and offset dimensions incorrect.

Reference

4/03.AI.455

for access panel locations.

boom utilities.

PM drop location per comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent change.

Equipment boom must be capable of providing all specified services, refer to Return of Submittal comment regarding Section R

Connect to nearest return duct above ceiling with airtight connection provisions, or delete boom utilities.VA/JVT: Please confirm if this is

PM location.

VA/JVT: Please advise. RFI 6735 sketch PL.X295 indicates two (2) CO2 for these booms. 26 55 71-01R3 indicates only one (1) CO2.

03.PP.103-A_JSI 118.3 corrected comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: September 1, 2015 Level: 03 - DAT Building 03 Rooms # OPERATING ROOM 4 ‐ ORTHO 03‐03‐G3‐02

SECTION I - LEVEL 3Clinical Solutions SECTION I -

R -A

/ce (30v

Prepared For: VA DENVER Date: November 04, 2014 Level: 03 Rooms# OPERATING ROOM 4-ORTHO 03-03-G3-02

Approved By: Approved By:

(Print) (Signature) control and wall controls per operative documents.

Access panel locations and offset dimensions incorrect.

Reference

4/03.AI.455

for access panel boom utilities.

PM drop location per comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent

Note changes.

capable of providing all specified services, refer to Return of Submittal comment regarding Section R

Connect to nearest return duct above ceiling with airtight connection provisions, or delete boom utilities.VA/JVT: Please confirm if this is

PM location.

VA/JVT: Please advise. RFI 6735 sketch PL.X295 indicates two (2) CO2 for these booms. 26 55 71-01R3 indicates only one (1) CO2.

Confirmed

03.PP.103-A_JSI 118.3 corrected comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: September 1, 2015 Level: 03 - DAT Building 03 Rooms # OPERATING ROOM 5 – DA VINCI / CYSTO 03‐03‐G2‐04

SECTION J - LEVEL 3Clinical Solutions SECTION J -

R -A

/ce (30v

Prepared For: VA DENVER Date: November 04, 2014 Level: 03 Rooms # OPERATING ROOM 5 - DA VINCI / CYSTO 03-03-G2-04

Approved By: Approved By:

(Print) (Signature) control and wall controls per operative documents.

Access panel locations and offset dimensions incorrect.

Reference

4/03.AI.455

(OPH.) for access panel boom utilities.

PM drop location per comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent changes.

Equipment boom must be capable of providing all specified services, refer to Return of Submittal comment regarding Section R

Connect to nearest return duct above ceiling with airtight connection provisions, or delete boom utilities.VA/JVT: Please confirm if this is

PM location.

VA/JVT: Please advise. RFI 6735 sketch PL.X296 indicates two (2) CO2 for these booms. 26 55 71-01R3 indicates only one (1) CO2.

Confirmed

03.PP.103-A_JSI 118.3 corrected

JVT to confirm if comments.

This room utilizes isolated power circuits clearly shown with separate home runs from the boom. Do not combine raceways where shown with independent

(Print)

Approved By: __________________________ (Signature) w w w . a m i c o . c o m

Prepared For: VA DENVER Date: August 24, 2015 Level:

Rooms #

3 - DAT, 5 - IBN, 9 - CBC

GENERAL DRAWINGS

SECTION M -

GENERAL DRAWINGSClinical Solutions SECTION M -

GENERAL DRAWINGS

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Prepared For: VA DENVER

Date: November 04, 2014

Level: 1 | 2 | 3 | 5 | 9

Rooms# GENERAL DRAWINGS

Approved By: Approved By:

(Print) (Signature)

Anchor plate assembly per Beckerle submittal.

Anchor plate assembly per Beckerle submittal.

Compact Design Allows for easy placement on a shelf or counter and accommodates stackability.

Quiet, Yet Powerful Operation Assists in providing a safe operating environment without disruption.

35 Hour Maximum Filter Life Delivers unsurpassed value and reduces per procedure costs.

3-Port Filter Design Puts the power of hose and accessory options in your hand and eliminates adapters.

Covered Filter Ports Filter ports are covered for additional safety.

Simplicity Reduces training needs and enhances utilization.

www.buffalofilter.com

ViroVac™ Surgical Smoke Plume Evacuator ViroVac" Surgical Smoke Plume Evacuator

BUFFALO

Filter

Compact Design Allows for easy placement on a shelf or counter and accommodates stackability.

Quiet, Yet Powerful Operation Assists in providing a safe operating environment without disruption.

35 Hour Maximum Filter Life Delivers unsurpassed value and reduces per procedure costs.

3-Port Filter Design Puts the power of hose and accessory options in your hand and eliminates adapters.

Covered Filter Ports Filter ports are covered for additional safety.

Simplicity Reduces training needs and enhances utilization.

World Leader in Surgical Smoke Evacuation as*0

A ViroSafe A

HP

V I www.buffalofilter.com

Buffalo Filter, LLC 5900 Genesee Street Lancaster, NY 14086 U.S.A.

Phone: 800.343.2324 (US) Phone: +1.716.835.7000 Fax: 716.835.3414

Email: smoke-info@buffalofilter.com Web: www.buffalofilter.com

*Nominal values Made in USA

PN 903209 REVC

ViroVac™ Surgical Smoke Plume Evacuator

Technical Information

Noise Levels* @ maximum power < 55 dBA

Dimensions (H x W x D) 6 in x 11 in x 15.5 in

15.2 cm x 27.9 cm x 39.4 cm

Flow Rates* 25 cfm (708 lpm) using 7/8 in (22 mm) tubing

Weight With filter installed: 12.0 lbs (5.0 kg) Without filter installed: 9.5 lbs (4.0 kg)

Warranty One (1) Year Full Warranty

Product Ordering Information

Catalog Number:

VV120 100/120 Volt Systems VV220 220/240 Volt Systems (includes one filter and one footswitch)

VV120 NF 100/120 Volt Systems VV220 NF 220/240 Volt Systems (includes one footswitch)

ViroVac™ is designed to be simple to use, flexible in its options for tubing and accessories, and sets new precedents for quiet operation. Providing effective surgical smoke plume evacuation that encompasses 4 layers of filtration and up to

35 hours of filter life, ViroVac™ will deliver the performance necessary to effectively manage surgical smoke plume with unsurpassed value.

EZLink, an automatic activation device (sold separately), can be used to remotely turn the evacuator on and off, saving filter life.

Buffalo Filter® is a registered trademark of Buffalo Filter, LLC in the United States and other countries. All other trademarks used herein are the property of their respective owners. ©2014. Buffalo Filter. All rights reserved.

EZLink (sold separately;

part: EZLINK01).

Pneumatic footswitch (included)

On/standby button

Service LED indicator

Footswitch port

Filter life indicator

Three motor speeds

Motor on/off indicator Sleep mode indicator

Three-port filter with hidden male ports

ViroVac" Surgical Smoke Plume Evacuator

ViroVac™ is designed to be simple to use, flexible in its options for tubing and accessories, and sets new precedents for quiet operation. Providing effective surgical smoke plume evacuation that encompasses 4 layers of filtration and up to 35 hours of filter life, ViroVac™ will deliver the performance necessary to effectively manage surgical smoke plume with unsurpassed value.

EZLink, an automatic activation device (sold separately), can be used to remotely turn the evacuator on and off, saving filter life.

Technical Information

Noise Levels* @ maximum power < 55 dBA

Dimensions (H x W x D) 6 in x 11 in x 15.5 in

15.2 cm x 27.9 cm x 39.4 cm

Flow Rates*

25 cfm (708 1pm) using 7/8 in (22 mm) tubing

Weight With filter installed: 12.0 lbs (5.0 kg) Without filter installed: 9.5 lbs (4.0 kg)

Warranty One (1) Year Full Warranty

Product Ordering Information

Catalog Number:

VV120 100/120 Volt Systems VV220 220/240 Volt Systems (includes one filter and one footswitch)

VV120 NF 100/120 Volt Systems VV220 NF 220/240 Volt Systems (includes one footswitch)

BUFFALO

Filter

World Leader in Surgical Smoke Evacuation"

Buffalo Filter, LLC 5900 Genesee Street Lancaster, NY 14086 U.S.A.

Phone: 800.343.2324 (US) Phone: +1.716.835.7000 Fax: 716.835.3414

Email: smoke-info@buffalofilter.com Web: www.buffalofilter.com

Motor on/off indicator Sleep mode indicator

On/standby button

B ViroSafe

Filter life indicator Service LED indicator

Three-port filter with hidden male ports

Pneumatic footswitch (included) EZLink (sold separately;

part: EZLINK01).

'Nominal values Made in USA

PN 903209 REVC

Buffalo Filter® is a registered trademark of Buffalo Filter, LLC in the United States and other countries. All other trademarks used herein are the property of their respective owners. ©2014. Buffalo Filter. All rights reserved.

Operator’s Manual

© 2011 BUFFALO FILTER®

5900 Genesee Street

Lancaster, New York USA 14086

(716) 835-7000 or (716) 835-3414 fax

Division of Medtek Devices, Inc.

Customer Service: 800-343-2324 (U.S. Only) – www.buffalofilter.com 1-716-835-7000 (International)

ViroVac™ Smoke Plume Evacuation System

Operator's Manual

BSg"0

ViroSafe m « I J, ViroVi ac a H-i

© 2011 BUFFALO FILTER®

5900 Genesee Street

Lancaster, New York USA 14086

(716) 835-7000 or (716) 835-3414 fax

Division of Medtek Devices, Inc.

Customer Service: 800-343-2324 (U.S. Only) - www.bulfalofilter.com 1-716-835-7000 (International)

Buffalo Filter ViroVac™ Operator’s Manual: Page 1

For a period of one (1) year following the date of delivery, BUFFALO FILTER warrants the Viro- Vac™ against any defects in material or workmanship. BUFFALO FILTER will repair or replace

(at BUFFALO FILTER’S option) the same without charge, provided that routine maintenance as specified in this manual has been performed using replacement parts approved by BUFFALO FILTER. This warranty is void if the product is used in a manner or for purposes other than intended.

© 2011 BUFFALO FILTER®

Lancaster, New York USA 14086

(716) 835-7000 www.buffalofilter.com

Division of Medtek Devices, Inc.

Customer Service: 800-343-2324 (U.S. Only) 1-716-835-7000 (International)

The revision level of this manual is specified by the highest revision letter found on either the inside front cover or enclosed errata pages (if any).

Manual Number 901837

Unit Serial Number ______________________

9D93

MEDICAL EQUIPMENT WITH RESPECT TO

ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY

IN ACCORDANCE WITH UL 60601-1 AND CAN/CSA C22.2 NO. 601.1

This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference and (2) this device must accept any interference received, including interference that may cause undesired operation.

For a period of one (1) year following the date of delivery, BUFFALO FILTER warrants the Viro- Vac™ against any defects in material or workmanship. BUFFALO FILTER will repair or replace

(at BUFFALO FILTER'S option) the same without charge, provided that routine maintenance as specified in this manual has been performed using replacement parts approved by BUFFALO FILTER. This warranty is void if the product is used in a manner or for purposes other than intended.

© 2011 BUFFALO FILTER®

Lancaster, New York USA 14086

(716) 835-7000 www.bufFalofilter.com

Division of Medtek Devices, Inc.

Customer Service: 800-343-2324 (U.S. Only) 1-716-835-7000 (International)

The revision level of this manual is specified by the highest revision letter found on either the inside front cover or enclosed errata pages (if any).

Manual Number 901837

Unit Serial Number

UL

9D93

MEDICAL EQUIPMENT WITH RESPECT TO

ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY

IN ACCORDANCE WITH UL 60601-1 AND CAN/CSA C22.2 NO. 601.1

This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference and (2) this device must accept any interference received, including interference that may cause undesired operation.

Buffalo Filter ViroVac™ Operator's Manual: Page 1

Buffalo Filter ViroVac™ Operator’s Manual: Page 2

Section Title Page

1.0 SYSTEM DESCRIPTION 3

1.1 Introduction

1.2 Inspection

1.3 Operational Information

1.4 Cautions and Warnings

2.0 OPERATING INSTRUCTIONS 10

2.1 System Controls

2.2 ViroSafe® Filter Instructions

2.3 Set-up and Operation

2.4 Specifications

3.0 MAINTENANCE 21

3.1 General Maintenance Information

3.2 Cleaning

3.3 Periodic Inspection

3.4 Troubleshooting

4.0 CUSTOMER SERVICE 22

4.1 Equipment Return

4.2 Ordering Information

5.0 TERMS & WARRANTY 23

Figure Title Page

1 Control Panel 14

Table of Contents & List of Illustrations

Table of Contents & List of Illustrations

Section Title Page

1.0 SYSTEM DESCRIPTION 3

1.1 Introduction

1.2 Inspection

1.3 Operational Information

1.4 Cautions and Warnings

2.0 OPERATING INSTRUCTIONS 10

2.1 System Controls

2.2 ViroSafe® Filter Instructions

2.3 Set-up and Operation

2.4 Specifications

3.0 MAINTENANCE 21

3.1 General Maintenance Information

3.2 Cleaning

3.3 Periodic Inspection

3.4 Troubleshooting

4.0 CUSTOMER SERVICE 22

4.1 Equipment Return

4.2 Ordering Information

5.0 TERMS & WARRANTY 23

Figure Title Page

1 Control Panel 14

Buffalo Filter ViroVac™ Operator's Manual: Page 2

Buffalo Filter ViroVac™ Operator’s Manual: Page 3

1.1 Introduction

BUFFALO FILTER® ViroVac™ Smoke Evacuation Systems are designed to remove smoke and noxious odors produced by surgical smoke during laser, electrosurgical, ultrasonic, argon, plasma and mechanical instrument procedures.

The ViroVac™ Smoke Evacuation Systems have been designed with a high suction, high flow rate centrifugal action pump. The ultra-quiet motor is used to draw the surgical smoke from the surgical site through the vacuum tubing and into the ViroSafe® filter where the surgical smoke is processed by a series of filters. A single disposable filter is used to simplify the installation and re-moval during filter changes. The filter is completely enclosed to protect the healthcare personnel from potential contamination during filter changes. One Buffalo Filter ViroSafe® filter contains four different stages within to capture the smoke plume.

The first stage filtration is a prefilter whose function is to trap and remove gross particulate and casual fluid.

The second stage filtration is ULPA grade (Ultra Low Penetration Air) filter whose high-tech patented (U.S. Patent #5874052) design captures particulates and micro-organisms from .1 to .2 microns at an efficiency of 99.999%.

The third stage filtration uses the highest grade virgin activated carbon, especially designed for Buffalo Filter for the removal and adsorption of odors and toxic gases produced by burning tis-sues. These harmful gases may constitute a health hazard to healthcare professionals who are subjected to prolonged exposure. The activated carbon used in the ViroVac™ Smoke Evacuation Systems preferentially removes toxic organic gases rather than water vapor and provides optimal odor removal.

The fourth stage filtration is an expanded foam used to trap activated carbon fines from migrating out of the filter.

The electronic controls on the face panel of the ViroVac™ Smoke Evacuation System has been designed “user friendly” and facilitate unit set up and operation. Please refer to Section 2.0 for Operating Instructions.

1.2 Inspection

The ViroVac™ Smoke Evacuator has been thoroughly tested and inspected before shipment from the factory. Please check the unit before using it to insure that no damage has occurred in transit.

If damage is evident, please contact BUFFALO FILTER Customer Service at 1-800-343-2324 (US Only) or (716) 835-7000 (International)

System Description Section 1.0

System Description Section 1.0

1.1 Introduction

BUFFALO FILTER® ViroVac™ Smoke Evacuation Systems are designed to remove smoke and noxious odors produced by surgical smoke during laser, electrosurgical, ultrasonic, argon, plasma and mechanical instrument procedures.

The ViroVac™ Smoke Evacuation Systems have been designed with a high suction, high flow rate centrifugal action pump. The ultra-quiet motor is used to draw the surgical smoke from the surgical site through the vacuum tubing and into the ViroSafe® filter where the surgical smoke is processed by a series of filters. A single disposable filter is used to simplify the installation and re moval during filter changes. The filter is completely enclosed to protect the healthcare personnel from potential contamination during filter changes. One Buffalo Filter ViroSafe® filter contains four different stages within to capture the smoke plume.

The first stage filtration is a prefilter whose function is to trap and remove gross particulate and casual fluid.

The second stage filtration is ULPA grade (Ultra Low Penetration Air) filter whose high-tech patented (U.S. Patent #5874052) design captures particulates and micro-organisms from .1 to .2 microns at an efficiency of 99.999%.

The third stage filtration uses the highest grade virgin activated carbon, especially designed for Buffalo Filter for the removal and adsorption of odors and toxic gases produced by burning tis sues. These harmful gases may constitute a health hazard to healthcare professionals who are subjected to prolonged exposure. The activated carbon used in the ViroVac™ Smoke Evacuation Systems preferentially removes toxic organic gases rather than water vapor and provides optimal odor removal.

The fourth stage filtration is an expanded foam used to trap activated carbon fines from migrating out of the filter.

The electronic controls on the face panel of the ViroVac™ Smoke Evacuation System has been designed "user friendly" and facilitate unit set up and operation. Please refer to Section 2.0 for Operating Instructions.

1.2 Inspection

The ViroVac™ Smoke Evacuator has been thoroughly tested and inspected before shipment from the factory. Please check the unit before using it to insure that no damage has occurred in transit.

If damage is evident, please contact BUFFALO FILTER Customer Service at 1-800-343-2324 (US Only) or (716) 835-7000 (International)

Buffalo Filter ViroVac™ Operator's Manual: Page 3

In addition, please compare the accessories you receive with the standard accessories list below. If an item is missing, please notify BUFFALO FILTER Customer Service.

Standard Accessories:

• Operator’s Manual

• Power Cord

• Pneumatic Footswitch

Please contact BUFFALO FILTER Customer…