S02 Attachment 17_N-SOU240607_3 Pages.pdf
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- 36C24826Q0453
About this file
This is a Philips equipment requirements document and installation planning guide for an Interventional Radiology (IR) laboratory renovation project at the US Veterans Administration Department of Veterans Affairs Medical Center in West Palm Beach, Florida.
The project involves installation of a Philips Azurion 7 C20 FlexArm imaging system with a 6000mm arm configuration. The equipment requirements package specifies critical environmental conditions including temperature maintenance between 59°F to 86°F with maximum gradient of 1°F per minute, humidity levels between 20% to 80% (non-condensing and stable within 10%), and HVAC heat load requirements of 5,456 BTU/hr for the exam room, 12,618 BTU/hr for the equipment room, and 1,944 BTU/hr for the control room. Electrical requirements mandate 100kW maximum rated power supplied via 3-phase, 380V to 480VAC at 60Hz with an 80A system circuit breaker and 100kVA branch power requirement. The document establishes responsibility matrices between Philips, the customer (VA Medical Center), contractors, and architects regarding site preparation, structural certification, permits, infection control compliance, radiation protection services, and hazardous material remediation. A comprehensive 52-week project timeline is provided detailing 18 sequential milestones from initial planning through project completion, including 3-week system delivery and installation, 16-week construction phase, and final inspections. Detailed site readiness checklists and inspection requirements are specified for floor preparation, electrical infrastructure, HVAC commissioning, equipment positioning, and compliance verification prior to equipment delivery. The project manager is Amar Subeir, contact (728) 202-5742, amar.subeir@philips.com. Drawing number N-SOU240607 A, dated 11/20/2024, is marked PROVISIONAL and includes architectural plans, general notes, and equipment layout specifications.
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www.healthcare.philips.com West Palm Beach, FL
C O
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S H
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*Photo shown is not site specific.
Important Note:
THE INFORMATION IN THIS PACKAGE IS PROVIDED AS PHILIPS EQUIPMENT REQUIREMENTS, AND IS NOT TO BE CONSTRUED AS ARCHITECTURAL DRAWINGS OR CONSTRUCTION DOCUMENTS.
Philips assumes no liability nor offers any warranty for the fitness or adequacy of the premises or the utilities available at the premises in which the equipment is to be installed, used, or stored.
For Architects and/or Contractors: The latest revision listed must be thoroughly reviewed so that all changes can be incorporated into your project, final revisions are valid for 90 days from latest revision date. Please check with Philips PM for current updates.
Rev. Date Revision Descriptions Planner CPM Approved By
- 9/13/2024 Created E-Plan. System upgraded to Rel. 3 from Rel. 2.2 reference project #: N-SOU240414. Jorge Valle Amar Subeir - A 11/20/2024 Updated background per CAD "WPB VA Renovate IR Cath Lab_Floor Plan 2024-11-12". Nicole Romero Amar Subeir
US Veterans Administration Dept.
of Veterans Affairs Medical Ctr.
Table of Contents Sheet Number Sheet Name
CS COVER SHEET
GN GENERAL NOTES
A1 ARCHITECTURAL PLANS
CS
THIS SHEET IS PART OF THE DOCUMENT SET LISTED ON SHEET CS
AND SHOULD NOT BE SEPARATED. 05.20.2024
K on in kl ijk e Ph ilip s
El ec tro ni cs N
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9.
A ll rig ht s re se rv ed . R ep ro du ct io n in w ho le o r i n pa rt is p ro hi bi te d w ith ou t p rio r w rit te n co ns en t o f t he co py rig ht h ol de r.
Project Details
Philips Contacts
Drawing Number
N-SOU240607 A
Date Drawn: 11/20/2024 Quote:
Order:
Pr oj ec t
U S
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A dm in is tr at io n
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Drawn By: Nicole Romero
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Project Manager:
Contact Number:
Email:
Amar Subeir
(728) 202-5742 amar.subeir@philips.com
G
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A
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These temperature and humidity levels must be maintained in all (3) rooms (equipment, examination and control rooms).
Temperature 59°F (15°C) to 86°F (30°C)
Temperature gradient Max. 1°F / Minute (0.5°C / Minute)
Humidity (non-condensing) Humidity shall be stable within 10% 20% to 80%
Exam Room *5456 BTU/hr
Equipment Room *12618 BTU/hr
Control Room *1944 BTU/hr
Electrical Requirements Mains MA Cabinet Maximum Rated Power: 100kW
Supply Configuration: 3 phase, equally sized insulated power conductors and an insulated equipment grounding conductor. Insulated grounding conductor shall have the same or larger size than line conductors. Line wires shall be no smaller than 4 AWG, 90°C or higher temperature rating. The conductor size is dependant on the upstream circuit breaker rating:
Nominal Line Voltage: 380 (Canada) - 480 VAC, 60 Hz
Branch Power Requirement: 100 kVA (System only; verify UPS power requirements)
Circuit Breaker: 3 phase, Type D with long-time delay and shunt trip Shunt trip to be removed when UPS is present.
System Circuit Breaker: 80A rating.
UPS breaker: 125A-150A, pending configuration.
(24.0)
Milestone and General Conditions for Successful IGT Projects
1. Planning, Design, and Implementation Process
The multidisciplinary project team should be assembled as early as possible in the design process. The multidisciplinary team should include administrators, clinicians, infection preventionists, architects and other design professionals, facility managers, safety officers, security managers, users of equipment, and support staff relevant to the areas affected by the project as well as those with knowledge of the organization's functional goal for the project. Inclusion of patient advocates/consumers, A/E consultants, and construction specialists should be considered. FGI (Facility Guidelines Institute) 2022 APPENDIX A1.2-1.2. (www.fgiguidelines.org) (Architect Responsible for ADA compliance.)
2. Schedule The customer or general contractor shall provide Philips with a project/construction schedule with milestones to assist in the coordination of delivery of Philips supplied products and primary equipment.
Project schedule must be provided by customer to obtain production slot and delivery.
3. Responsibility The customer shall be solely responsible, at their expense for preparation of site. Philips required specifications and any required MEP, construction and structural alterations shall be incorporated into customer's design and construction documents. Compliance with all safety, electrical, and building design codes relevant to the build out of the clinical area for Philips equipment and its installation is the customer's responsibility. Sufficiency of such plans and specifications, specifically including, but not limited to the accuracy of the dimensions described therein, shall be the sole responsibility of the customer. The customer shall advise Philips of conditions at or near the site, which could adversely affect the function of the equipment and/or carrying out of the delivery and installation work.
a. Customer's structural engineer shall provide Philips with written certification that structural supports meet Philips requirements to permit delivery and installation of equipment.
b. Customer shall acknowledge the final site preparation confirmation document.
c. Upon completion of project, Customer's Architect and Engineers of record shall provide a set of As-Built project construction documents (.dwg) to Philips for closure of the Philips project history file.
This shall ensure that such conditions are compliant and that the site is fully prepared and available for Philips before the installation work is due to begin.
4. Permits Customer shall obtain all permits and licenses required by federal, state/provincial or local authorities in connection with the construction, installation and operation of the products and shall bear any expense in obtaining same or in complying with any related rules, regulations, ordinances and statutes.
5. Infection Control and Interim Life Safety Measure The customer shall provide all means and methods necessary for compliance with Infection Control (IC) and Interim Life Safety Measures (ILSM) in connection with the construction and installation/operation of the products shown herein and shall bear any expenses related to same.
6. Radiation Protection The customer or their contractor, at their own expense, shall obtain the service of a licensed radiation physicist to specify radiation protection and testing.
7. Asbestos and Other Toxic Substances Philips assumes that there is no hazardous material contained in the project site. The customer is responsible for the removal of any materials, including but not limited to asbestos, deemed hazardous by local authorities, the EPA, OSHA, or any other authority having jurisdiction over the work. If such materials are discovered at any time that the work is proceeding, the work will immediately cease, the owner will be notified, and the work will again proceed after the owner has removed all of the hazardous material from the job site.
8. Labor In the event local labor conditions make it impossible or undesirable to use Philips' regular employees for such installation and connection, such work shall be performed by laborers supplied by the customer, or by an independent contractor chosen by the customer at the customer's expense, and in such case, Philips agrees to furnish adequate technical support and supervision for proper completion for the Philips equipment installation.
9. Extended Installation or Turnkey Work by Philips If an extended installation or turnkey contract exists between Philips and the customer for room preparation some of the responsibilities of the customer as depicted in these drawings may be assumed by Philips. In the event of a conflict between the work described in the turnkey contract work scope and these drawings, the turnkey contract work scope shall govern.
10. Boom Vendors/3rd party cables Separation of cables shall be provided by boom vendor for the installation of cables within the boom. For example, use of liquid-tight plastic conduit.
(24.0)
INSPECTIONS
Inspected by: Date:
Facilities:
Clinical:
Infectious Control:
Architect:
Engineer:
Administrator:
Project Manager:
Sales Specialist:
Account Manager:
Service:
REQUIRED SITE READINESS CHECK LIST FOR PHILIPS DELIVERY
Items to be completed Prior to Equipment Delivery: Inspected by: Date: Common Site Drawing Reference:
Sheet/Section/Detail
Table Iso Center: Verified per Philips Final Drawings. A1/1,2.
Floor Levelness: Checked with Laser Level. S1/1, S1/Equipment Support Information.
Floor Plates: installed, isolated, and leveled at the correct locations. S1/1,3, S1/Equipment Support Information.
Ceiling Unistruts (P1001): Installed and leveled per Sheet with written engineer certification. S2/2,6,7,8, S2/Equipment Support Information.
Modular Laminar Array with Unistruts (P1001) installed and level per sheet if Class 3 required. S2/7, S2/Equipment Support Information.
Ceiling Plate for Equipment Rack (EP Boom) (if applicable): Installed and leveled.
Cable Trough/Raceway/Conduit: Greenlee measuring tape (part no. 435, or equivalent) are Installed, verified and locations checked. E1/Point to Point Run Lengths, E1/1,4.
3rd Party Booms (if applicable): Structural support installed and verified with boom vendor and locations.
Ceiling Height: Verified and measure from bottom of Unistrut. S2/2,7.
Verify the Fixing Blocks sits properly in the Unistrut channel with no obstructions. S2/6,8.
Ceiling Obstructions: Verify there are no obstructions where Philips rails will be installed. S2/1,3.
Clearances: Verified to the closest obstacles (i.e. walls, cabinets), in order to lift up the C-arm, monitor support, etc. AD1/1.
Back Boxes: Installed with required covers and grommet material. E1/1, ED/4,5.
ERB Conductor Bar Installed per drawing. E1/1,2.
All electrical boxes and raceway are grounded to the ERB. ED/1,2,5,6.
Mains Power Supply: Installed per drawing (Including impedance, isolated grounds, wire size and circuit breakers verified). ED/Power Quality Requirements (Azurion), ED/Branch Circuit and Wire Gauge Requirement (Azurion).
Mains Supply Wiring installed for connection in Cabinet Rear Cover (CRC) of MA-Cabinet. ED/5,6.
Video Connection Boxes: video sources, and display destinations are verified with customer and located. A1/AUX Chart.
Med Gas Box (if applicable): Location does not interfere with the installation and movement of table. S1/3,5.
Walls: Installed and final finished per customers architectural specifications.
Millwork: Completely installed in all rooms.
Leaded glass installed.
Flooring: Installed and covered with protective covering (1/8" masonite). S1/Equipment Support Information.
Lighting and Wall Outlets Installed and functional. ED/General Electrical Information.
HVAC system is operational and commissioned to engineered specifications. GN/HVAC Requirement for General Equipment Locations.
3rd Party Booms (if applicable): Installed prior to Philips equipment delivery.
UPS: Fully installed per Philips Final Drawings, and startup has been scheduled with vendor. ED/6.
X-Ray in Use Light is installed. ED/3.
Physicist: If required has been scheduled.
UPS: Commissioned and certified by UPS vendor.
Permits Inspections: Completed or scheduled by applicable governing authorities.
All network information provided by facility IT, i.e. IP addresses (static IPs only), AE Titles, SNM, GTWY and DNS server are available. NN.
Project Space: Is clean, free of dust, all construction-related debris and tools have been removed.
PPE requirements identified (Construction and Hospital). No open electrical or hazardous materials on site. GN/Milestone and General Conditions for Successful IGT project.
Site Access Is available for after hours. Storage for tools, parts, covers and packing material has been arranged.
Room is secure with keys provided.
Complete Delivery Path Route and backup for bad weather has been reviewed & reverfied with the customer and lead FSE.
(24.0)
(24.0)
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Milestones and Tasks for Successful IGT a Single Suite Project
ID
Task Name
IGT Single Suite Project
Hospital Multidisciplinary Project Team Planning with AM and CPM (Project Initial Schedule)
Philips P.O. Issued
Architect/Engineering Phase (Experienced Design Build 6-8 Weeks/Standard AE 8-16 Weeks)
Construction Bidding and Award (Depends on Complexity)
Final Defined Project/Construction Schedule Review Meeting with CPM, Hospital PM, GC
Philips Secures Production Slot and Determines Delivery Date
Permitting - DOH/CON Approvals (Local Permits 1-4 Weeks)
Mobilization - MEP Lead Times (HVAC System and Airframe "Hybrid" 8-24 Weeks)
Removal of Old Equipment (3 Days)
Construction Phase (Based on Complexity and Site Constraints - Average 16 Weeks)
Philips System Delivery and Installation (3 Weeks Average)
Hospital 3rd Party Delivery and Installation (Booms, Hemo, Laser, Ultrasound, Video Integration)
14 Final Inspections (Philips Certification, Radiation Physicist, Fire Marshal, Cert. of Occupancy, etc.)
Terminal Cleaning and Stocking
Clinical Training - First Patient
Non-Standard System Acceptance Terms and Conditions (Govt 45 Days from Inspection Notice or Other Special Terms)
18 Project Complete (Sale Record Date)
Duration
52.4 wks
4 wks Hospital Multidisciplinary Project Team Planning with AM and CPM (Project Initial Schedule)
1 wk Philips P.O. Issued
8 wks Architect/Engineering Phase (Experienced Design Build 6-8 Weeks/Standard AE 8-16 Weeks)
4 wks
0.2 wks
Construction Bidding and Award (Depends on Complexity)
Final Defined Project/Construction Schedule Review Meeting with CPM, Hospital PM, GC
0.8 wks
4 wks
4 wks
Philips Secures Production Slot and Determines Delivery Date
Permitting - DOH/CON Approvals (Local Permits 1-4 Weeks)
Mobilization - MEP Lead Times (HVAC System and Airframe "Hybrid" 8-24 Weeks)
1 wk Removal of Old Equipment (3 Days)
16 wks Construction Phase (Based on Complexity and Site Constraints - Average 16 Weeks)
3 wks Philips System Delivery and Installation (3 Weeks Average)
2 wks Hospital 3rd Party Delivery and Installation (Booms, Hemo, Laser, Ultrasound, Video Integration)
2 wks Final Inspections (Philips Certification, Radiation Physicist, Fire Marshal, Cert. of Occupancy, etc.)
1 wk
1 wk
0.2 wks
Terminal Cleaning and Stocking
Clinical Training - First Patient
Non-Standard System Acceptance Terms and Conditions (Govt 45 Days from Inspection Notice or Other Special Terms)
0.2 wks Project Complete (Sale Record Date)
1 54
Remote Control of Room Lighting Room lighting controls are the responsibility of the customer. Refer to sheet ED/2 for X-ray in use and room light switching requirements.
(24.0)
HVAC Requirement for General Equipment Locations
*Average heat emission during clinical use Data applicable for basic system:
Large monitor + 4 x small monitor in Monitor Ceiling Suspension 1 workstation + 2 x small monitor in Control Room
Add 8750 BTU/hr for Optional Socomec UPS Add 1194 BTU/hr for additional large monitor Add 273 BTU/hr for additional small monitor Add 1024 BTU/hr for additional workstation See AD details for additional heat load in case of UPS and Ambient
Equipment's designed airflow is from front/side to back. Please design the air handling in the rack cabinet equipment area accordingly.
Philips IGT-S systems may only be operated at an altitude of max. 9,843 ft (3,000m) above sea level as defined in our instructions for use (IFU).
(24.0)
GN
THIS SHEET IS PART OF THE DOCUMENT SET LISTED ON SHEET CS
AND SHOULD NOT BE SEPARATED. 05.20.2024
K on in kl ijk e Ph ilip s
El ec tro ni cs N
.V . 2
9.
A ll rig ht s re se rv ed . R ep ro du ct io n in w ho le o r i n pa rt is p ro hi bi te d w ith ou t p rio r w rit te n co ns en t o f t he co py rig ht h ol de r.
Project Details
Philips Contacts
Drawing Number
N-SOU240607 A
Date Drawn: 11/20/2024 Quote:
Order:
Pr oj ec t
U S
Ve te ra ns
A dm in is tr at io n
D ep t.
of
V et er an s A ffa irs
M ed ic al
C tr
W es t P al m
B ea ch , F
L R oo m
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L ab
D ra w in g Ti tle
None None
U S
Ve te ra ns
A dm in is tra tio n D ep t.
of V et er an s
Af fa irs M ed ic al C tr.
W es t P al m
B ea ch , F
L
Drawn By: Nicole Romero
TH
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Project Manager:
Contact Number:
Email:
Amar Subeir
(728) 202-5742 amar.subeir@philips.com
AVO NAMING
Line Item Corresponding Naming
FCV0972 (powered by system, in control room) AVOC
FCV0973 (powered by system, in exam room) AVOE
FCVO974 (powered by hospital) AVOX
FCV0975 (4K AVO) AVOK
FCV0976 (XL) AVOL
Integration Kits AVOB
FlexVision Non-Philips Frame AVOM
AD7 Table Floor Plate ℄
C le a / T ab le
Iso Center The Iso Center is the initial and most crucial control point in the construction of a procedure room.
Once established, it guides the placement of all imaging equipment, third-party devices, mechanical, electrical, and plumbing systems (MEPs), as well as the overall construction. These are positioned relative to the Iso Center's X, Y, and Z coordinates to avoid operational issues and clinical limitations.
14'-4" 4367mm
'-8 m m
2'-1" 635mm
8'-0" 2438mm
'-1
1 8" m m
4' -6 m m
7'-6" 2286mm
11'-4" 3454mm
'-9 m m
32'-71 8"
9935mm
'-1
1" m m
1 2"
7m m 3'
-1
0m m
3'-1" 940mm
1'-91 2"
547mm
2'-21 8"
664mm 2'-9" 838mm
3'-95 8"
1159mm
3' -9
5 8" m m
2' -9
3 4"
6m m
2'-93 4"
856mm
4'-21 8"
1273mm
4' -2
1 8" m m
2' -0
1 4"
6m m
2' -1
5m m
1' -5
3 8"
1m m
2' -6
1 8"
5m m
MA
MB
ME
AD7 Table Floor Plate ℄
C le a / T ab le
℄ C us to m er 's
P hy si o
(P H
Y)
CY
O pt io na l ( U
PS
C oo rd in at e fin al lo ca tio n w ith cu st om er if or de re d
AUX8
Service area to meet NEC/ESA requirement
3'-61 8"
1070mm
4' -0 m m
CR1
AUX1
AUX2
AUX3
AUX4
AUX5
AUX6
AUX7
14'-4" 4367mm
SH
Iso Center
ATY
Exact location to be coordinated by Customer and local Philips service.
DB
VB9
VB10
AD7
Safety Zone
Safety Zone
CC
Ceiling Inlet
FVXL
FVXL2
3'-4" 1016mm
'-8 m m
A
B C
IH
Ceiling Inlet
Safety Zone
Safety Zone
7'-13 4"
2178mm
5'-31 8"
1602mm
4" 99mm
2' -7
5 8"
4m m
81 4"
0m m
3' -3
3 8" m m Elevation check needed
Min. distance for boomsUse this area only when boom can fit between bottom of rails and of vertical arm.
x-ax is
C en te r l in e of Tr an sv er sa l m ov em en t
Vertical Arm
Min. distance for booms. Use this area only when boom can fit between bottom of hybrid cable arm and vertical arm.
<8 1 4" b ot to m o f
Fl ex
Ar m c ab le du ct a rm
No fly zone
Elevation check needed
Hybrid cable duct Hybrid cable arm
2'-103 8"
873mm
1' -6
1 2"
0m m
2'-03 4"
627mm
4'-7" 1396mm
Patient Right Patient Left
5'-3" 1600mm
5'-3" 1600mm
Fi ni sh ed fl oo r t o bo tto m o f u pp er d ec k he ig ht
9' -6
1 2"
1 8" (2
8m m
3m m
U ni st ru t h ei gh t m ea su re d fro m fi ni sh ed fl oo r t o bo tto m o f U ni st ru t.
Se e de ta il
S2 /1
No fly zone
To p of ve rti ca l ar m
'-1
1" m m
33'-6" 10211mm
AD7 Table Floor Plate ℄ 18'-11" 5765mm
14'-7" 4445mm
C le a / T ab le
'-1 11 2" m m
'-1
11 2" m m
4'-0" 1220mm
4'-0" 1219mm
4' -0 m m
4'-0" 1219mm
4' -0 m m 2'
-6
2m m
2' -6
2m m
1'-6" 457mm
1'-6" 457mm
1'-6" 457mm
1'-6" 457mm
Walls
Soffit
Existing (to be removed)
Beams or other building construction elements
Legend
A R
C H
IT
EC
TU
R
A L
PL
A
N S
A AD7 Angio Diagnost 7 Table 992 450
A ME Certeray iX Generator Cabinet 320 145
A MA Mains 40E Cabinet 717 325
A DB Documentation Box - Mounted on Wheels (Final location to be coordinated with customer and/or local Philips Service)
176 80
A ATY Exam Room Auxiliary Box 7 3
A IH Interventional Hardware 73 33
A MB Image 40E Cabinet 497 225
A AUX1 Auxiliary Equipment Adapter 4 2
A AUX10 Auxiliary Equipment Adapter 4 2
A CR1 Control Room Equipment Adapter 4 2
A SH Service Hub 7 3
Items not on Philips Quote/Order
SCALE:
Required Unistrut Height: 9' - 61
2", ±1 8" (2908mm, ±3mm) Unistrut height measured from finished floor to bottom of Unistrut.
A1
SITE LAYOUT
3/16" = 1' - 0"
SCALE:
A1
ELEVATION (Not Site Specific)
1/4" = 1' - 0"
* Architect to coordinate with end users/technicians to determine final placement of control desk components prior to installation in order to avoid rework. Architect to coordinate with Philips Project Manager to reflect final placement on Philips drawings.
Important Notes:
* Field to verify all room dimensions by customer and Philips
Important Notes:
Minimum FGI Area for Movable Equipment
Minimum FGI Area for Circulation Pathway
Sterile Field 8'x16' (2438mm x 4877mm)
Legend
Anesthesia Zone 6'x8' (1829mm x 2438mm)
SCALE:
A1
FGI GUIDELINES CLASS 3 (Not Site Specific)
3/16" = 1' - 0"
(24.0)
(24.0)
(24.0)
A FVXL MCS - SpringArm - 300mm 1068 485
A FVXL2 MCS - SpringArm - 300mm 1068 485
A CC Clea Ceiling 2755 1250
Source Location Displayed
AUX1 Physio Control FlexVision
AUX2 Physio Control FlexVision
AUX3 FlexSpot/Growth ** Control FlexVision
AUX4 PACS** Control FlexVision
AUX5 IH Control FlexVision
AUX6 INT** Control FlexVision
AUX7 SYNC** Control FlexVision
AUX8 Anesthesia** Exam FlexVision
AUX9
Procedure
Equipment** Exam FlexVision
AUX10
Procedure
Equipment** Exam FlexVision
* Sources shown below are for consideration only.
Sources may change per quote/order.
Table Movement Ceiling Equipment Movement Table Pinch Hazard
Legend
Service Area Required Ventilation
SCALE:
Required Unistrut Height: 9' - 61
2", ±1 8" (2908mm, ±3mm) Unistrut height measured from finished floor to bottom of Unistrut.
A1
EQUIPMENT LAYOUT
3/16" = 1' - 0"
A1
THIS SHEET IS PART OF THE DOCUMENT SET LISTED ON SHEET CS
AND SHOULD NOT BE SEPARATED. 05.20.2024
K on in kl ijk e Ph ilip s
El ec tro ni cs N
.V . 2
9.
A ll rig ht s re se rv ed . R ep ro du ct io n in w ho le o r i n pa rt is p ro hi bi te d w ith ou t p rio r w rit te n co ns en t o f t he co py rig ht h ol de r.
Project Details
Philips Contacts
Drawing Number
N-SOU240607 A
Date Drawn: 11/20/2024 Quote:
Order:
Pr oj ec t
U S
Ve te ra ns
A dm in is tr at io n
D ep t.
of
V et er an s A ffa irs
M ed ic al
C tr
W es t P al m
B ea ch , F
L R oo m
: I R
L ab
D ra w in g Ti tle
None None
U S
Ve te ra ns
A dm in is tra tio n D ep t.
of V et er an s
Af fa irs M ed ic al C tr.
W es t P al m
B ea ch , F
L
Drawn By: Nicole Romero
TH
E
IN
FO
R M
AT
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Project Manager:
Contact Number:
Email:
Amar Subeir
(728) 202-5742 amar.subeir@philips.com
Existing to be MovedH
Equipment Designation
Description
Equipment Legend
Optional Future Existing Furnished by Philips and installed by contractor Installed by customer/contractor Furnished by customer/contractor and installed by customer/contractor
G
D C B
Furnished and installed by PhilipsA
F E
Furnished by Philips and installed by Philips 3rd PartyI
Weight (lbs)
Weight (kg)
Detail Sheet
B A Boom A - -
B B Boom B - -
B C Boom C - -
Conduit run(s) from SP to MA/MR must be able to take the most direct route.
(Maximum distance point to point = 36")
Planning Issues and Considerations
Third Party Items - It is the customer's responsibility to interface and coordinate all non-Philips' item(s) / equipment to ensure full functionality and movement of all equipment.
Boom layout shown is based on a reference design. Final boom placement to be discussed between customer and 3rd Party Vendor.
A CY Control Room Junction Box 73 33
General Notes
* Exact equipment configuration to be verified with local Philips Sales.
Patient loading may be difficult. Verify with customer requirement.
Potential collision of equipment with noted cabinet / wall.
4!
| Sheets and Views |
| N-SOU240607-CS |
| N-SOU240607-GN |
| N-SOU240607-A1 |
File details come from the government source that posted it. Updated .