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SOLICITATION/CONTRACT/ORDER FOR COMMERCIAL ITEMS
OFFEROR TO COMPLETE BLOCKS 12, 17, 23, 24, & 30
1. REQUISITION NUMBER PAGE 1 OF
2. CONTRACT NO. 3. AWARD/EFFECTIVE
DATE
4. ORDER NUMBER 5. SOLICITATION NUMBER 6. SOLICITATION ISSUE
DATE
7. FOR SOLICITATION
INFORMATION CALL:
a. NAME b. TELEPHONE NUMBER (No collect calls)
8. OFFER DUE DATE/
LOCAL TIME
9. ISSUED BY
13b. RATING
14. METHOD OF SOLICITATION
CODE
15. DELIVER TO 16. ADMINISTERED BY CODE
18a. PAYMENT WILL BE MADE BY CODE 17a. CONTRACTOR/
OFFEROR
CODE
FACILITY
CODE
CODE
TELEPHONE NO.
17b. CHECK IF REMITTANCE IS DIFFERENT AND PUT SUCH ADDRESS IN
OFFER
18b. SUBMIT INVOICES TO ADDRESS SHOWN IN BLOCK 18a UNLESS BLOCK
BELOW IS CHECKED
RFQ IFB RFP
SEE ADDENDUM
19.
ITEM NO.
20.
SCHEDULE OF SUPPLIES/SERVICES
21.
QUANTITY
22.
UNIT
23.
UNIT PRICE
24.
AMOUNT
(Use Reverse and/or Attach Additional Sheets as Necessary)
25. ACCOUNTING AND APPROPRIATION DATA 26. TOTAL AWARD AMOUNT (For Govt. Use Only)
28. CONTRACTOR IS REQUIRED TO SIGN THIS DOCUMENT AND RETURN
DELIVER ALL ITEMS SET FORTH OR OTHERWISE IDENTIFIED ABOVE AND ON ANY
ADDITIONAL SHEETS SUBJECT TO THE TERMS AND CONDITIONS SPECIFIED
29. AWARD OF CONTRACT: REF.
DATED . YOUR OFFER ON SOLICITATION
(BLOCK 5), INCLUDING ANY ADDITIONS OR CHANGES WHICH ARE
SET FORTH HEREIN, IS ACCEPTED AS TO ITEMS:
30a. SIGNATURE OF OFFEROR/CONTRACTOR
30b. NAME AND TITLE OF SIGNER (Type or print) 30c. DATE SIGNED
31a. UNITED STATES OF AMERICA (SIGNATURE OF CONTRACTING OFFICER)
31b. NAME OF CONTRACTING OFFICER (Type or print) 31c. DATE SIGNED
AUTHORIZED FOR LOCAL REPRODUCTION
PREVIOUS EDITION IS NOT USABLE
STANDARD FORM 1449 (REV. 3/2005)
Prescribed by GSA - FAR (48 CFR) 53.212
10. THIS ACQUISITON IS
UNRESTRICTED OR
NAICS:
SIZE STANDARD:
COPIES TO ISSUING OFFICE. CONTRACTOR AGREES TO FURNISH AND
OFFER
13a. THIS CONTRACT IS A
RATED ORDER UNDER
DPAS (15 CFR 700)
SET ASIDE: % FOR:
SMALL BUSINESS
HUBZONE SMALL
BUSINESS
SERVICE-DISABLED VETERAN-
OWNED SMALL BUSINESS
EMERGING SMALL
BUSINESS
8(A)
11. DELIVERY FOR FOB DESTINA-
TION UNLESS BLOCK IS
MARKED
SEE SCHEDULE
12. DISCOUNT TERMS
ARE ARE NOT ATTACHED
ARE ARE NOT ATTACHED
27a. SOLICITATION INCORPORATES BY REFERENCE FAR 52.212-1, 52.212-4. FAR 52.212-3 AND 52.212-5 ARE ATTACHED. ADDENDA
27b. CONTRACT/PURCHASE ORDER INCORPORATES BY REFERENCE FAR 52.212-4. FAR 52.212-5 IS ATTACHED. ADDENDA
SP0200-06-R-8014 Page 2 of 217
TABLE OF CONTENTS
FOR
Patient Monitoring Systems, Subsystems, Accessories, Consumables, Spare/Repair Parts, Training and Maintenance Services
SOLICITATION: SP0200-06-R-8014
TITLE PAGE
Caution Notice (if any) None
Standard Form (SF) 1449, Solicitation/Contract/Order for Commercial Items 1
Solicitation Response Sheet for No Offer 3 Continuation of any block(s) from SF 1449-- Block 8 - Offer Due Date/Local Time 4 Block 10 – This Acquisition Is 4 Block 17a – Contractor / Offeror 4 Block 17b - Remittance Address 4 Blocks 19-24 - Schedule of Supplies/Services/Prices 5
Contract Clauses--
1. FAR clause 52.212-4, Contract Terms and Conditions--Commercial Items 88
2. Addendum to 52.212-4 88
3. FAR clause 52.212-5, Contract Terms and Conditions Required to
Implement Statutes or Executive Orders--Commercial Items 131
4. Addendum to 52.212-5 DFARS clause 252.212-7001 Contract Terms and Conditions Required to Implement Statutes or Executive Orders Applicable to Defense Acquisitions of Commercial Items 136
Any contract documents, exhibits or attachments-- 174 - 198
Solicitation Provisions--
1. FAR provision 52.212-1, Instructions to Offerors--Commercial Items 139
2. Addendum to 52.212-1 139
(b) Submission of Offers
(c) Period for acceptance of offers
(e) Multiple offers
(h) Multiple Awards
3. [x] FAR provision 52.212-2, Evaluation--Commercial Items 151 [ ] Addendum to 52.212-2, Evaluation Criteria (Continuation Sheet)
4. FAR provision 52.212-3, Offeror Representations and Certifications - 152 Commercial Items
5. Addenda to 52.212-3 DFARS provision 252.212-7000, Offeror Representations and Certifications-- 199 Commercial Items
6. Addendum – Subcontracting Plan Outline 209
SP0200-06-R-8014 Page 3 of 217
For: Patient Monitoring Systems, Subsystems, Accessories, Consumables, Spare/Repair Parts, Training and Maintenance Services
[ ] CANNOT COMPLY WITH SPECIFICATION
[ ] CANNOT MEET DELIVERY REQUIREMENT
[ ] NO OPEN PRODUCTION CAPACITY AT PLANT
[ ] DO NOT REGULARLY MANUFACTURE OR SELL TYPE OF ITEMS INVOLVED
[ ] OTHER (SPECIFY)
[ ] WE DO [ ] WE DO NOT DESIRE TO BE RETAINED ON THE MAILING LIST FOR
FUTURE PROCUREMENT OF THE TYPE OF ITEM(S) INVOLVED
NAME AND ADDRESS OF FIRM (INCLUDE ZIP CODE)
TYPE OR PRINT NAME AND TITLE OF SIGNER
SIGNATURE
SP0200-06-R-8014 Page 4 of 217
ADDENDUM TO STANDARD FORM 1449
1. Continuation of Block 8
This is a solicitation from which the Government contemplates award of multiple customer value contracts (CVC) for Patient Monitoring Systems, Subsystems, Accessories, Consumables, Spare/Repair Parts, Training and Maintenance Services. Offerors are requested to submit complete proposals for all requirements, including all certifications, as specified in this solicitation. Proposals may be submitted at any time during the solicitation period. (See 52.212-2 Evaluation – Commercial Items (Jan 1999) Tailored at page 151.
Offer Due Date/Local Time: April 19, 2007, 2:00 P.M. Eastern Daylight Time
2. Continuation of Block 10: NAICS CODES include but are not limited to 337910, 339111, 339112, 339113, 339114, 339115, 339116, 334516, 334510, 421460, 33999 and 421740.
3. Continuation of Block 17a:
Offeror’s assigned DUNS Number: _______________________.
4. Continuation of Block 17b:
Remittance Address is: ___________________________
Note: The Government will mail checks to this address only in the event of an Electronic Funds Transfer (EFT) failure, pursuant to 52.232-33 (which is incorporated by reference at 52.212- 5(b)(31)).
5. CAGE Number: ___________
6. Are you registered with the Central Contractor Registration (CCR) database?
Yes [ ] No [ ]
(If you have not registered or your registration has expired, please visit the website at www.ccr.gov) http://www.ccr.gov/
SP0200-06-R-8014 Page 5 of 217
ADDENDUM TO STANDARD FORM 1449 (continued)
6. Continuation of Blocks 19-24:
SCHEDULE OF SUPPLIES/SERVICES
The offeror shall include with his offer two (2) copies (one (1) electronic and one
(1) hard copies) of established commercial price lists, catalog, or other documentation setting forth the prices charged the general public for the items. In addition, two (2) hard copies and one (1) electronic copy of the completed solicitation shall be included with the offer.
Offerors are highly recommended to segregate their commercial price lists, catalog, technical data and/or cost and pricing data to facilitate Government review.
Offerors shall submit uniform or a reasonably limited number of discounts from list price per product category, i.e. System Options, Consumable & Accessories, Upgrades.
Offerors shall provide with their offer a computerized record of all proposed items documented in Microsoft Word for Windows 6.0. The source documents for the applicable sections may be located at DSCP’s World Wide Web site at http://www.dscp.dla.mil via the Medical Home Page. Although the document and amendments may be viewed through this media, downloads are not currently supported. Accordingly, the electronic document may be obtained via disk through the Contracting Officer.
Offerors shall furnish their current list price, offered discount, and net price offered on both an individual component and system basis for each component and system offered.
Offers on percentage discounts from list prices that vary from year to year are not requested or acceptable. Offerors shall submit offers as discounts from list price for the first contract year only. Economic Price Adjustments to the first year prices will apply for contract years 2 through 10. Thus all offerors, to be acceptable, must submit only Base Year prices (list price minus discount) with any changes to the award prices in the first year and all other years determined by the application of the EPA Clause and the “Specials or Discounts” paragraph on page 13.
Offerors are encouraged to include in their offer all product line items, accessories and services with respect to the subject equipment modality.
http://www.dscp.dla.mil/
SP0200-06-R-8014 Page 6 of 217
Offerors may use the sample pricing chart included in the solicitation on the following pages or the vendor may submit their own catalog pricing pages, as long as all DSCP requested information is available. If the offeror provides their own pricing pages, the offeror must identify the pricing page number for each item on the System Identification Charts.
Offerors shall furnish two (2) copies of complete technical data for each product line item, accessory and service submitted with their offer. Technical data shall include all commercially available image quality and physics data currently available, including a description of any test phantoms, software or other test equipment used to measure such data.
Offered schedules of supplies, list prices, offered discounts from list prices and the resulting net prices are for the Base Year of the forthcoming contract.
Offered discounts from the base list prices may not be reduced (but may be increased by the contractor) during the life of the contract.
Base year prices may be adjusted only as authorized by the March 2006 Economic Price Adjustment (EPA) clauses incorporated in this solicitation and the “Specials or Discounts” paragraph. Price increases are limited to the annual percentage ceiling(s) specified in the EPA clauses. See page 98 for additional information.
Notwithstanding any other clauses of this contract, at any time during the contract, any contract unit price may not exceed the FSS (Federal Supply Schedule) price, minus any Veteran Administration surcharges paid as a result of a FSS sale (e.g., the VA’s Industrial Funding Fee of 0.5%), in effect at that time.
SP0200-06-R-8014 Page 7 of 217
1. Requirement:
Monitoring Systems and Subsystems:
1. Bedside Monitoring System
2. Configured Bedside Monitoring System
3. Fetal Bedside Monitoring System
4. Transport (Vital Signs) Monitoring System
5. Central Monitoring System
6. Specialty Monitoring System
7. Full Disclosure Systems
8. Cardiology Analysis Systems
9. Clinical Information Systems
10. Telemetry Systems
11. Telemetry Patient Locator Systems
12. Nurse Paging Systems
13. Electroencephalographs (EEG)
14. Networking/Interfacing
The Government is soliciting for strictly commercial material in accordance with the Federal Acquisition Streamlining Act (FASA) FAR Part 12 “Commercial Items.”
As part of their proposals, offerors will be asked to submit pricing for turnkey installation and training requirements as described within the specification.
The estimated total dollar value of this acquisition, $254,000,000.00, is based upon the average taken from actual sales over the last 4 ½ years, multiplied by the projected number of years for the duration of these proposed contracts, and includes a projection of additional funds for “special projects”, as well as inflationary factors.
2. TERM:
This solicitation proposes to establish an indefinite delivery/indefinite quantity contract for monitoring systems and subsystems. The term of the contract will be a one-year base with (9) one-year options.
SP0200-06-R-8014 Page 8 of 217
3. AWARD:
The solicitation is being issued pursuant to FAR Part 16.5 “Multiple Awards”. For this particular acquisition, the Government may award contracts to all responsible firms who offer technically acceptable commercial products. Provision 52.216-27 “Single or Multiple Awards for Delivery Order Contracts” will be incorporated into the solicitation. Acceptability for award necessitates that individual vendors have the following criteria:
1. FDA approval on all systems;
2. Submission of two (2) copies of technical data for each product line item, accessory, and service submitted with their offers;
3. Market acceptability, i.e., item in clinical use for not less than six (6) months for at least one (1) clinical site;
4. Offerors must agree to all terms and conditions of the solicitation.
4. MINIMUM/MAXIMUM:
The guaranteed minimum dollar value shall be the cost of one system, subsystem, or component. In the solicitation, contractors will be advised to provide the Government with past government sales history as well as an estimate of what they think their maximum sales under this proposed contract will be. This information will be used to arrive at a maximum dollar threshold for each offeror.
5. MULTIPLE AWARDS:
The Government plans to award multiple contracts for the same or similar supplies under this solicitation. This will enable DSCP to better serve customer needs through its ability to offer a variety of items relative to an individual customer’s needs or clinical requirements. If an offeror meets the terms and conditions of the solicitation, as well as those other factors cited in #3 – AWARD, an award will be made to this firm.
6. DELIVERY ORDERS:
The Government will place delivery orders with the contract awardee(s) representing the most advantageous offer to the requiring activity for that specific ordering requirement. Prior to the placement of each delivery order, a customer will justify its rationale for selecting its chosen source for the required supplies.
Such documentation need not be submitted to the ordering activity (DSCP).
Evaluation factors for delivery orders, to be included in the solicitation, are as follows:
(a) Clinical Performance/User Considerations
(b) Past Performance
(c) Delivery
(d) Price
Delivery Orders will be negotiated on those items specific to a particular site.
SP0200-06-R-8014 Page 9 of 217
7. NEW PRODUCTS:
Vendors can offer new products or substitutions of obsolete products with authorization through the Procurement Contracting Officer. See page 14 “Changes for Substitute and/or Upgrade Items”.
8. “PROMOTION” PRICES:
DSCP will allow vendors to offer promotions of items for a specific price at a specified period of time, e.g. sales and promotions, etc. This will be accomplished by issuing a modification to the contract stipulating that the price of these items will be reduced by a stipulated dollar value for a specified time period. These “promotional items” will then be marketed along with those items currently on the contract.
9. PRICING
The offered schedules of supplies, list prices, offered discounts from list prices, and the resulting net prices are for the Base Year (first year) of this contract only.
The offered discounts from list prices may not be reduced (but may be increased by the contractor) during the life of the contract. Prices may be decreased at any time in accordance with the Economic Price Adjustment (EPA) Clause and/or the “Specials or Discounts” paragraph on page 15. Base year prices may be adjusted (increased) only as authorized by the EPA clause and or the “Specials or Discounts” paragraph of the solicitation. Price increases are limited to the annual percentage ceiling specified in the EPA clause.
The prices for each of the nine one-year options are the same as the first or base year prices awarded under the contract. The consecutive years’ prices may be adjusted only as authorized by the Economic Price Adjustment (EPA) Clause and/or the “Special or Discounts” Provision incorporated in the solicitation. The net contract unit prices for any consecutive year(s) may not exceed the previous contract year by more than the annual ceiling on upward price adjustments set forth in the EPA clause.
A price increase ceiling of 10% per year is currently imposed in the EPA Clause and is the Government’s desired maximum limit. Offerors may propose lower or higher ceilings that would either apply to all items or different ceilings for different categories of items. If different ceilings are offered for different categories of items, these categories must be consistent with the different categories of items and offered list price discounts offered in a vendor’s response to this solicitation and should be kept to a reasonable number. Any offered price ceilings in excess of 10% may be subject to the negotiation.
SP0200-06-R-8014 Page 10 of 217
NOTICE TO OFFERORS
A. Minimum/Maximum Quantity
1. The minimum contract quantity shall consist of 1 system (i.e. multiple networked monitors), subsystem (i.e. individual equipment or monitor) or accessory, of our choosing, of those offered.
2. The estimated maximum quantity shall be * systems/subsystems/component or accessories.
B. Your attention is directed to point 7 “Delivery Orders” on pages 11 and 12 of the solicitation.
C. If you project your dollar figure to exceed $550,000.00 for this contract and you are not a Small
Business, your company is required to submit a Small Business Subcontracting Plan as set forth in FAR clause 52.219-9.
D. The vendor shall address exceptions in a separate cover.
NOTE: ALL ITEMS SUPPLIED SHALL BE NEW, ORIGINAL MANUFACTURER ITEMS. THEY
SHALL NOT CONSIST OF ANY RECONDITIONED, REBUILT, REMANUFACTURED,
ETC. ITEMS.
* The vendor shall propose a maximum quantity or dollar value for this contract.
The vendor shall provide a justification for this dollar value. In addition, the vendor shall provide their last year’s sales to the DOD and or Federal Government.
SP0200-06-R-8014 Page 11 of 217
SOLICITATION/CONTRACT/ORDER FOR COMMERCIAL ITEMS --SF1449
(CONTINUATION SHEET)
1. REQUIREMENT. Monitoring Systems and Subsystems.
2. TERM. This solicitation proposes to establish an indefinite delivery/quantity contract for the offered items. The terms of the contract will be 1 Base Year and 9 Option Years. See the following clauses:
CLAUSE NO. TITLE PAGE
52.216-18 Ordering 94 52.216-19 Order Limitations 95 52.216-22 Indefinite Quantity 96
3. FOB Offers are solicited on a FOB CONUS Destination basis only. The following locations will be considered OCONUS unless otherwise specified: Puerto Rico, Alaska, and Hawaii. The vendor may be required to provide equipment and services to OCONUS location.
4. SUBMISSION OF OFFERS. For instructions on how to submit offers, i.e., what information must be included in proposals, see provision 52.212-1, Instructions to Offerors - Commercial Items.
5. OPEN SEASONS: This solicitation will result in a long term contract consisting of a base term and one or more option terms (provided the Government invokes one or more of the term options associated with each contract awarded). Therefore, additional offers from NEW SUPPLIERS ONLY will be considered for a thirty day period beginning sixty days before the end of each contract term. The Government reserves the right not to award a contract to any new offeror proposing to supply an item already on contract or at a price not considered fair and reasonable. Any resulting contracts awarded under this provision will run for the same period of time remaining as in the original contract awards.
6. AWARD. The Government may award contracts to all responsible firms who are considered to be technically acceptable, whose pricing is determined to be fair and reasonable, and who meet all other terms and conditions of the solicitation*. See provision 52.216-27 “Single or Multiple Award”.
* See Market Acceptability Criteria.
7. MINIMUM/MAXIMUM. (Note that the following minimum, annual estimate, and maximum quantities assume multiple awards.)
The annual estimate for this solicitation is $25,400,000.00. The guaranteed minimum is one (1) system/subsystem/component for the base year, as well as for each of the nine (9) remaining option years. The maximum dollar value for this solicitation is *. Contractors are cautioned that the Government estimates are the most accurate the Government can develop at this time; however, the Government assumes no responsibility if the actual requirements ordered under any resulting contracts are more or less than the estimates. In order for the Government to manage extraordinary demand in requirements and to preclude backorder problems, the Government reserves the right to exceed the estimated yearly quantity up to the maximum quantity shown for each of the ten (10) program years.
* The vendor shall propose a maximum dollar value for this contract. The vendor shall provide a justification for this dollar value. At a minimum, the vendor shall provide their last year sales to the Government. The vendor is encouraged to provide their last three years of sales history to the Government.
7. DELIVERY ORDERS.
a. Delivery Orders will be issued for shipments to the customers as the need materializes. Orders may be placed in accordance with the clauses cited in paragraph 2 above and with the basic policy stated below.
SP0200-06-R-8014 Page 12 of 217
b. Basic Policy. The Government will place delivery orders with the contract awardee who represents the most advantageous offer to the requiring activity for the specific requirement being ordered. For each requirement, the most advantageous will be determined from the population of existing contracts by considering the following evaluation factors, in accordance with the needs of the requiring activity.
(1) Clinical Performance/User Considerations
(2) Past Performance
(3) Delivery
(4) Price
The evaluation factors shall be applied to each requirement by the requiring activity as part of the process in determining who is to receive a delivery order.
c. The Government will order supplies by issuing delivery orders during the period specified in 52.216-18, Ordering. Each delivery order will contain, as a minimum:
(1) Purchase Request/Requisition No.
(2) Date of Order
(3) Contract number, order number
(4) Contract line item number (CLIN), (if applicable), National Stock
Number (NSN, (if applicable) and Item Description
(5) Quantity
(6) Unit Price
(7) Accounting and appropriation data
(8) Delivery date
(9) Inspection and acceptance information
8. SCHEDULE OF DELIVERIES OR PERFORMANCE. The delivery time is nominally established as 30 to 120 days after the date of award of the delivery order. The exact required delivery date (RDD) shall be specified on each delivery order. The Contracting Officer shall not specify, without further negotiations, delivery dates which exceed the contract expiration date plus the number of days offered in the delivery schedule.
9. Please note that this contract will result in (1) Base Year and (9) Option Years.
10. This acquisition is not being solicited on an “All Or None” basis. Vendors are advised that they can elect to offer on various configurations of this system/subsystem. If an offeror does not elect to bid on a particular line item, it is requested that this be clearly indicated by annotating “No Bid” to this line item.
11. Offeror shall supply 2 hard copies and the price list in electronic format (Word, Excel, Access, etc.)
12. Solicitation will be made available via the web at www.dscp.dla.mil http://www.dscp.dla.mil/
SP0200-06-R-8014 Page 13 of 217
Special Notes
• Offerors are reminded the following:
• Pricing must be addressed for the base year.
• Delivery schedules must be addressed for all items offered.
• This acquisition is not being solicited on an “all or none” basis. Vendors are advised that they can elect to offer on various configurations of the systems/subsystems described in this solicitation. If an offeror does not elect to bid on a particular item, it is requested that this be clearly indicated by annotating “NO BID” for that item.
Contract Documents/Attachments
CHANGES FOR SUBSTITUTE AND/OR UPGRADE ITEMS
The Government reserves the right to issue changes for substitute items to incorporate product upgrades.
Award will be made for the make and model offered. If the contractor upgrades its product line or enhances an awarded line item after award, substitutions may be permitted only with the express written consent of the Contracting Officer. Generally, substitutions will only be permitted at no additional cost. Substitutions, if approved, will be effective for orders issued after the aforementioned consent is provided.
If optional accessories are added to contractor’s product line after award, such accessories may be added to the contract only with the express written consent of the Contracting Officer. The contractor shall submit a proposal including product descriptions and proposed prices to the Contracting Officer.
SPECIALS OR DISCOUNTS
Contractors may offer “specials” or “discounts” at any time during the term of the contract. Once the “special” or “discount” period expires, prices will revert to the contract price(s) in effect for that term.
TRADE-IN POLICY
Contractors may offer “trade-ins” of existing equipment at any time during the term of the contract.
These trade-ins will be advertised to our customers. If our customer has an item to trade-in, either DSCP and/or the customer will contact the contractor to determine the terms and conditions of the trade-in at time of inquiry. If the contractor offers a trade-in under the existing contract, the terms and conditions of the trade-in must be forwarded to the Contracting Officer. The letter must state at a minimum the Model Number of the trade-in and the dollar credit for the trade-in towards the purchase of the new equipment. The letter must be signed by the Contractor.
SP0200-06-R-8014 Page 14 of 217
Option Year Pricing/Discount Description Notice to Offerors
Please complete the system identification charts below with the offered percentage off list price, per individual system description, for the base year. Shaded cells ($>>>>areas) do not need to be completed.
Percent Discount Off List Price (%) System Description*
Base Year
01. Bedside Monitoring System
01A.
Modular Bedside Monitoring System.
01AA.
Modular Bedside Monitoring System, Color.
01AB.
Modular Bedside Monitoring System, Monochrome or Other Non-Color
01B.
Parameter Modules – Modular Bedside Monitors.
02.
Configured Bedside Monitoring System.
02A.
Configured Bedside
02AA.
Configured Bedside Monitoring
SP0200-06-R-8014 Page 15 of 217
System Description*
Base Year
02AB.
Configured Bedside Monitoring System, Monochrome or Other
03. Fetal
Monitoring System.
03A. Fetal Bedside
03AA. Fetal
Monitoring
03AB. Fetal
Monitoring System, Monochrome or Non-Color
04.
Transport (Vital Signs) Monitoring
04A.
(Vital Signs)
04AA.
(Vital Signs) Monitoring
04AB.
(Vital Signs) Monitoring System, Monochrome or Other
SP0200-06-R-8014 Page 16 of 217
Base Year
04AC.
Transport (Vital Signs) Monitoring System, Army Aero- Medical Certification.
04AD.
(Vital Signs) Monitoring System, Air Force Aero-
04AE.
(Vital Signs) Monitoring System, Army & Air Force Aero-
05. Central
System.
05A. Central Bedside
05AA.
Central Bedside Monitoring
05AB.
Bedside Monitoring System, Monochrome or Other
05B. Central Fetal
SP0200-06-R-8014 Page 17 of 217
Base Year
05BA.
Central Fetal Monitoring
05BB.
Central Fetal Monitoring System, Monochrome or Other
05C. Central Telemetry
05CA.
Telemetry Monitoring
05CB.
Telemetry Monitoring System, Monochrome or Other
06.
Specialty Monitoring System.
06A.
Cardiac Catherization
06AA.
Cardiac Catherization Monitoring
SP0200-06-R-8014 Page 18 of 217
Base Year
06AB.
Cardiac Catherization Monitoring System, Monochrome or Other Non- Color System.
06B.
Angiographic
06BA.
Monitoring
06BB.
Monitoring System, Monochrome
06C.
Magnetic Resonance
06CA.
Resonance
System, Color
06CB.
Resonance Monitoring System, Monochrome
SP0200-06-R-8014 Page 19 of 217
Base Year
06D.
Anesthesia
06DA.
Anesthesia
06DB.
Anesthesia
System, Color.
07. Full Disclosure Systems.
08. Cardiology Analysis Systems.
08A. Automated External Defibrillators
(AED)
08B.
Electrocardiographs
(ECG)
08C. Other Cardiology Acquisition Devices and Accessories (Holter, Stress, Treadmills, etc.)
08D. Management
09. Clinical Information Systems.
10. Telemetry
11.
Electroencephalograph (EEG) Systems
12. Networking/ Interfacing
12A.
Networking/Interfacing Of Existing Equipment
12B.
Of New Equipment
12C.
Of New Equipment to Existing Equipment
13. Trade-In >>>>
14. Upgrade Of Existing Equipment
15. Extended Installation
16. Turnkey >>>>
SP0200-06-R-8014 Page 20 of 217
Installation
17. Extended Warranty
18. Training. >>>> 18A. Operator Training
18B. Maintenance Training
19. Provisioning >>>>
*Note: Shaded cells (& >>>> areas) do not need to be completed.
Table of Contents
01. BEDSIDE MONITORING SYSTEM.
01A. Modular Bedside Monitoring System.
01AA. Modular Bedside Monitoring System, Color.
01AB. Modular Bedside Monitoring System, Monochrome or Other Non-Color System.
01B. Parameter Modules - Modular Bedside Monitors
02. CONFIGURED BEDSIDE MONITORING SYSTEM.
02A. Configured Bedside Monitoring System.
02AA. Configured Bedside Monitoring System, Color.
02AB. Configured Bedside Monitoring System, Monochrome or Other Non-Color System.
03. FETAL BEDSIDE MONITORING SYSTEM.
03A. Fetal Bedside Monitoring System.
03AA. Fetal Bedside Monitoring System, Color.
03AB. Fetal Bedside Monitoring System, Monochrome or Other Non-Color System.
04. TRANSPORT (VITAL SIGNS) MONITORING SYSTEM.
04A. Transport (Vital Signs) Monitoring System.
04AA. Transport (Vital Signs) Monitoring System, Color.
04AB. Transport (Vital Signs) Monitoring System, Monochrome or Other Non-Color System.
04AC. Transport (Vital Signs) Monitoring System, Army Aero-medical Certification 04AD. Transport (Vital Signs) Monitoring System,, Air Force Aero-medical Certification 04AE. Transport (Vital Signs) Monitoring System, Army and Air Force Aero-medical
Certification
05. CENTRAL MONITORING SYSTEM.
05A. Central Bedside Monitoring System.
05AA. Central Bedside Monitoring System, Color.
05AB. Central Bedside Monitoring System, Monochrome or Other Non-Color System.
05B. Central Fetal Monitoring System.
05BA. Central Fetal Monitoring System, Color.
05BB. Central Fetal Monitoring System, Monochrome or Other Non-Color System.
05C. Central Telemetry Monitoring System.
05CA. Central Telemetry Monitoring System, Color.
SP0200-06-R-8014 Page 21 of 217
05CB. Central Telemetry Monitoring System, Monochrome or Other Non-Color System.
06. SPECIALTY MONITORING SYSTEM.
06A. Cardiac Catherization Monitoring System.
06AA. Cardiac Catherization Monitoring System, Color.
06AB. Cardiac Catherization Monitoring System, Monochrome or Other Non-Color System.
06B. Angiographic Monitoring System.
06BA. Angiographic Monitoring System, Color.
06BB. Angiographic Monitoring System, Monochrome or Other Non-Color System.
06C. Magnetic Resonance Monitoring System 06CA. Magnetic Resonance Monitoring System, Color.
06CB. Magnetic Resonance Monitoring System, Monochrome or Other Non-Color System.
06D. Anesthesia Monitoring System.
06DA. Anesthesia Monitoring System, Color.
06DB. Anesthesia Monitoring System, Monochrome or Other Non-Color System.
07. FULL DISCLOSURE SYSTEMS.
08. CARDIOLOGY ANALYSIS SYSTEMS.
08A. Automated External Defibrillators (AED) 08B. ECG – Electrocardiographs 08C. Other Cardiology Acquisition Devices and Accessories (Holter, Stress, Treadmills, etc.)
08D. Management Systems
09. CLINICAL INFORMATION SYSTEMS.
10. TELEMETRY SYSTEMS.
11. ELECTROENCEPHALOGRAPH (EEG) SYSTEMS
12. NETWORKING/INTERFACING.
12A. Networking/Interfacing Of Existing Equipment 12B. Networking/Interfacing Of New Equipment
12C. Networking/Interfacing Of New Equipment to Existing Equipment
13. TRADE-IN.
14. UPGRADE OF EXISTING EQUIPMENT.
15. EXTENDED INSTALLATION.
16. TURNKEY INSTALLATION.
17. EXTENDED WARRANTY
18. TRAINING.
SP0200-06-R-8014 Page 22 of 217
18A. Operator Training 18B. Maintenance Training
19. PROVISIONING
01. BEDSIDE MONITORING SYSTEM.
01A. Modular Bedside Monitoring System.
01AA. Modular Bedside Monitoring System, Color.
01AB. Modular Bedside Monitoring System, Monochrome or Other Non-Color System.
01AC Provide a listing of all other available options and accessories:
SP0200-06-R-8014 Page 23 of 217
Item: 01A Description: Modular Bedside Monitoring System
DSCP
IQC
ITEM #
CATALOG
PAGE REF
VENDOR
CATALOG
NUMBER
DESCRIPTION LIST
PRICE ($)
DISC
NET PRICE
COUNTRY OF
ORIGIN
SP0200-06-R-8014 Page 24 of 217
01B. Parameter Modules - Modular Bedside Monitors
A variety of parameter modules shall be available for use with the modular bedside monitors.
Please list below the parameter modules that are available. Please specifically note if the parameter modules may be used with other monitoring systems such as transport monitors, fetal monitors, etc.
SP0200-06-R-8014 Page 25 of 217
Item: 01B Description: Parameter Modules - Modular Bedside Monitors
DSCP
IQC
ITEM #
CATALOG
PAGE
REF
VENDOR
CATALOG
NUMBER
DESCRIPTION LIST
PRICE ($)
DISC
NET PRICE
SP0200-06-R-8014 Page 26 of 217
02. CONFIGURED BEDSIDE MONITORING SYSTEM.
02A. Configured Bedside Monitoring System.
02AA. Configured Bedside Monitoring System, Color.
02AB. Configured Bedside Monitoring System, Monochrome or Other Non-Color System.
02AC Provide a listing of all other available options and accessories:
SP0200-06-R-8014 Page 27 of 217
Item: 02 Description: Configured Bedside Monitoring System.
DSCP
IQC
ITEM #
CATALOG
PAGE
REF
VENDOR
CATALOG
NUMBER
DESCRIPTION LIST
PRICE ($)
DISC
NET PRICE
SP0200-06-R-8014 Page 28 of 217
03. FETAL BEDSIDE MONITORING SYSTEM.
03A. Fetal Bedside Monitoring System.
03AA. Fetal Bedside Monitoring System, Color.
03AB. Fetal Bedside Monitoring System, Monochrome or Other Non-Color System.
03AC Provide a listing of all other available options and accessories:
SP0200-06-R-8014 Page 29 of 217
Item: 03 Description: Fetal Bedside Monitoring System.
DSCP
IQC
ITEM #
CATALOG
PAGE
REF
VENDOR
CATALOG
NUMBER
DESCRIPTION LIST PRICE ($) DISC
NET PRICE
SP0200-06-R-8014 Page 30 of 217
04. TRANSPORT (VITAL SIGNS) MONITORING SYSTEM.
04A. Transport (Vital Signs) Monitoring System.
04AA. Transport (Vital Signs) Monitoring System, Color.
04AB. Transport (Vital Signs) Monitoring System, Monochrome or Other Non-Color System.
04AC. Transport (Vital Signs) Monitoring System, Army Aeromedical Certification.
The Transport (Vital Signs) Monitoring System shall be designed to pass Aeromedical Certification requirements and must be in Compliance with the following standards. Military standards shall be interpreted as though all units will be used aboard military aircraft.
a. Electrical Safety Evaluations. The unit will not exceed the leakage current and ground resistance limits in AFI 41-203, Electrical Shock Hazards, which reference National Fire Protection Agency (NFPA) 99.
b. Environmental Testing to MIL-STD-810E.
Test Method Test Criteria
501.3 High Temperature Operation 49oC/15 percent
RH/2 hrs
Procedure II The medical device will operate correctly at temperatures up to and including 49oC.
501.3 High Temperature Storage 71oC/15 percent
RH/6 hrs
Procedure I The medical device will operate after being stored in a high temperature environment (71oC).
SP0200-06-R-8014 Page 31 of 217
Test Method Test Criteria
502.1 Low Temperature Operation -25oC/na/2 hrs
Procedure II at -25oC.
502.1 Low Temperature Storage -46oC/na/6 hrs
Procedure I The medical device will operate correctly after being stored in a low temperature environment (-46oC).
507.3 Humidity 29.5oC/95 percent
Procedure I RH/4 hrs The medical device will operate correctly in a high humidity and high temperature environment.
500.3 Altitude 15,000 ft. for 1 hr.
in a low pressure environment (15,000 foot altitude equivalent).
514.4 Vibration 2.116 Grams each axis for 1 Hr
Procedure The medical device will operate correctly in a vibration environment. Currently tested in each of three different axes in accordance with the procedure noted.
c. Electromagnetic Characteristics Testing to MIL-STD-461C limits:
Method Frequency and/or V/m CE03 30Hz - 50kHz CE03 10kHz - 50kHz
SP0200-06-R-8014 Page 32 of 217
CE04 50kHz - 50MHz
The medical device shall not produce conducted emissions in excess of current MIL-STD-461C limits.
Method Frequency and/or V/m CS02 50kHz - 400MHz CS06 spikes of 200 V/m
The medical device shall not be susceptible to MIL-STD-461C test generated power spikes or signals induced on its power lines.
RE02 14kHz - 12.4GHz
The medical device shall not produce radiated emissions in excess of current MIL-STD-461C limits.
RS03 10kHz - 10GHz (20 V/m)
The medical device shall not be susceptible to radiated test fields produced to MIL-STD-461C levels.
d. Electromagnetic characteristics testing is conducted in accordance with current MIL-STD-462 methods to current MIL-STD- 461C limits. Testing includes applicable conducted emissions and susceptibility as well as radiated emissions and susceptibility testing.
e. In-Flight Testing. A flight evaluation can only be performed after laboratory evaluations are completed and an airworthiness is obtained from ATCOM.
f. The medical device shall operate according to the performance test criteria in the aircraft without limitations due to environmental factors, including noise. The operator will be able to operate the medical device through it's full range of functions while wearing the flight ensemble, including gloves and a flight helmet. The medical device shall not interfere with any aircraft system. The medical device shall not be susceptible to interference from aircraft systems.
g. Army Aeromedical Test Standards listed above shall be performed at:
U.S. Army Aeromedical Research Laboratory (USAARL)
SGRD-UAD-IE
Ft. Rucker, Alabama 36362.
04AD. Transport (Vital Signs) Monitoring System, Air Force Aeromedical Certification.
SP0200-06-R-8014 Page 33 of 217
220V, 50 Hz 110V, 60 Hz
The Transport (Vital Signs) Monitoring System shall be designed to pass Aeromedical Certification requirements and must be in Compliance with the following standards. Military standards shall be interpreted as though all units will be used aboard Military aircraft.
a. Electromagnetic Interference (EMI). The purpose of the EMI tests is to verify compliance with MIL-STD-461D and MIL-STD-462D, "Electromagnetic Emission and Susceptibility Requirements for the Control of Electromagnetic Interference" and "Measurement of EMI Characteristics, respectively.
1. Radiated Emissions (RE-102) - This test measures radiated emissions generated by the unit. Excessive emissions could interfere with aircraft navigation and communication equipment. The unit is tested while operating on each possible power source that it is configured for, such as internal rechargeable battery, 110VAC/60Hz, 110VAC/400Hz, and 28VDC.
2. Radiated Susceptibility (RS-103) - This test determines whether the ambient electromagnetic fields encountered in flight interfere with the operation of the unit. During exposure to the electromagnetic induction fields the unit is operated on each possible power source that it is configured for, such as internal rechargeable battery, 110VAC/60Hz, 110VAC/400Hz, and 28VDC.
3. Conducted Emissions (CE-102) - This test measures emissions generated by the unit and conducted back up the power line. Excessive conducted emissions could affect the aircraft power supply and/or other systems powered from it. The unit is tested while operating on each possible power source that it is configured for, such as 110VAC/60Hz, 110VAC/400Hz, and 28VDC, except for internal battery.
4. Conducted Susceptibility (CS-101) - This test verifies that the unit will safely operate during allowable fluctuations in the aircraft's power supply. During the exposure the unit is tested while operating on each possible power source that it is configured for, such as 110VAC/60Hz, 110VAC/400Hz, and 28VDC, except for internal battery.
5. Conducted Susceptibility (CS-114) - This test verifies that the unit will safely operate during current fluctuations along its cables. During the exposure the unit is tested while operating on each possible power source that it is configured for, such as 110VAC/60Hz, 110VAC/400Hz, and 28VDC, except for internal rechargeable battery.
6. Conducted Susceptibility (CS-115) - This test verifies that the unit will safely operate during transients in the aircraft's power supply. During the exposure the unit is tested while operating on each possible power source that it is configured for, such as 110VAC/60Hz, 110VAC/400Hz, and 28VDC, except for internal rechargeable battery.
b. Vibration. MIL-STD-810E, Environmental Test Methods and Engineering Guidelines, are followed to test the unit's construction, durability, performance, and the integrity of the mounting device while withstanding random vibration and sinusoidal vibration on the X, Y, and Z axes.
SP0200-06-R-8014 Page 34 of 217
c. Environmental. MIL-STD-810E, the numerical values listed below do not come from any MIL-STD or other source document.
They are modified versions of those in MIL-STDs, and simulated operational conditions. Environmental testing is performed under the following test conditions:
1. Humidity Operation: 94 + 4 percent relative humidity, 85oF + 3.6oF (29.5oC + 2oC) for four hours.
2. Hot Temperature Operation: 120oF + 3.6oF (49oC + 2oC) for two hours.
3. Cold Temperature Operation: 32oF + 7.2oF (0oC+ 4oC) for two hours.
4. Hot Temperature Storage: 140oF + 3.6oF (60oC+ 2oC) for six hours.
5. Cold Temperature Storage: -40oF + 3.6oF (-40oC + 4oC) for six hours.
d. Altitude. MIL-STD-810E, each unit is subjected to reduced atmosphere pressures from 522.7 mmHg, 10,000 ft equivalent in a hypobaric chamber. The exposure time varies with the equipment item under evaluation, but is usually a minimum of 1 hour.
e. Rapid Decompression. Decompressions in flight are uncommon; however, if one were to occur, the unit should not present a hazard to the patient, crew or aircraft operations. Each unit is subjected to a series of rapid decompression (RD) tests, starting at an equivalent pressure altitude of 8,000 ft. with subsequent changes of altitude to 40,000 ft over periods of 60, 7, and 1 second.
f. Airborne Feasibility. Primary objectives of this phase are to identify problems with the unit that could not be evaluated in the lab, assess human factors in the aircraft environment (in accordance with MIL-STD-1472D), assess ease of loading the unit on the aircraft, ensure visibility of visual alarms and audibility of audible alarms, check aircraft interface and unit securing methods, and assess the effect of the combined stresses of flight on the unit.
g. Air Force Aeromedical Test Standards listed above shall be performed at:
Armstrong Laboratory/CFTS Aeromedical Research Function 2504 D. Drive, Suite 1 Brooks AFB, Texas 78235-5104
04AE. Transport (Vital Signs) Monitoring System, Army and Air Force Aero-medical Certification.
220V, 50 Hz 110V, 60 Hz
The Transport (Vital Signs) Monitoring System shall be designed to pass Aero-medical Certification requirements and must be in Compliance with the following standards. Military standards shall be interpreted as though all units will be used aboard military aircraft.
SP0200-06-R-8014 Page 35 of 217
a. Electrical Safety Evaluations. The unit will not exceed the leakage current and ground resistance limits in AFI 41-203, Electrical Shock Hazards, which reference National Fire Protection Agency (NFPA) 99.
b. Environmental Testing to MIL-STD-810E.
Test Method Test Criteria
501.3 High Temperature Operation 49oC/15 percent
RH/2 hrs
Procedure II at temperatures up to and including 49oC.
501.3 High Temperature Storage 71oC/15 percent
RH/6 hrs
Procedure I The medical device will operate after being stored in a high temperature environment (71oC).
502.1 Low Temperature Operation -25oC/na/2 hrs
Procedure II at -25oC.
502.1 Low Temperature Storage -46oC/na/6 hrs
Procedure I The medical device will operate correctly after being stored in a low temperature environment (-46oC).
507.3 Humidity 29.5oC/95 percent
Procedure I RH/4 hrs The medical device will operate correctly in a high humidity and high temperature environment.
500.3 Altitude 15,000 ft. for 1 hr.
SP0200-06-R-8014 Page 36 of 217 in a low pressure environment (15,000 foot altitude equivalent).
514.4 Vibration 2.116 Grams each axis for 1 Hr
Procedure The medical device will operate correctly in a vibration environment. Currently tested in each of three different axes in accordance with the procedure noted.
c. Electromagnetic Characteristics Testing to MIL-STD-461C limits:
CE03 30Hz - 50kHz CE03 10kHz - 50kHz CE04 50kHz - 50MHz
The medical device shall not produce conducted emissions in excess of current MIL-STD-461C limits.
Method Frequency and/or V/m CS02 50kHz - 400MHz CS06 spikes of 200 V/m
The medical device shall not be susceptible to MIL-STD-461C test generated power spikes or signals induced on its power lines.
Method Frequency and/or V/m RE02 14kHz - 12.4GHz
The medical device shall not produce radiated emissions in excess of current MIL-STD-461C limits.
Method Frequency and/or V/m RS03 10kHz - 10GHz (20 V/m)
The medical device shall not be susceptible to radiated test fields produced to MIL-STD-461C levels.
d. Electromagnetic characteristics testing is conducted in accordance with current MIL-STD-462 methods to current MIL-STD- 461C limits. Testing includes applicable conducted emissions and susceptibility as well as radiated emissions and susceptibility
SP0200-06-R-8014 Page 37 of 217 testing.
e. In-Flight Testing. A flight evaluation can only be performed after laboratory evaluations are completed and an airworthiness is obtained from ATCOM.
f. The medical device shall operate according to the performance test criteria in the aircraft without limitations due to environmental factors, including noise. The operator will be able to operate the medical device through it's full range of functions while wearing the flight ensemble, including gloves and a flight helmet. The medical device shall not interfere with any aircraft system. The medical device shall not be susceptible to interference from aircraft systems.
g. Army Aeromedical Test Standards listed above shall be performed at:
U.S. Army Aeromedical Research Laboratory (USAARL)
SGRD-UAD-IE
Ft. Rucker, Alabama 36362.
h. Electromagnetic Interference (EMI). The purpose of the EMI tests is to verify compliance with MIL-STD-461D and MIL-STD- 462D, "Electromagnetic Emission and Susceptibility Requirements for the Control of Electromagnetic Interference" and "Measurement of EMI Characteristics, respectively.
1. Radiated Emissions (RE-102) - This test measures radiated emissions generated by the unit. Excessive emissions could interfere with aircraft navigation and communication equipment. The unit is tested while operating on each possible power source that it is configured for, such as internal rechargeable battery, 110VAC/60Hz, 110VAC/400Hz, and 28VDC.
2. Radiated Susceptibility (RS-103) - This test determines whether the ambient electromagnetic fields encountered in flight interfere with the operation of the unit. During exposure to the electromagnetic induction fields the unit is operated on each possible power source that it is configured for, such as internal rechargeable battery, 110VAC/60Hz, 110VAC/400Hz, and 28VDC.
3. Conducted Emissions (CE-102) - This test measures emissions generated by the unit and conducted back up the power line. Excessive conducted emissions could affect the aircraft power supply and/or other systems powered from it. The unit is tested while operating on each possible power source that it is configured for, such as 110VAC/60Hz, 110VAC/400Hz, and 28VDC, except for internal battery.
4. Conducted Susceptibility (CS-101) - This test verifies that the unit will safely operate during allowable fluctuations in the aircraft's power supply. During the exposure the unit is tested while operating on each possible power source that it is configured for, such as 110VAC/60Hz, 110VAC/400Hz, and 28VDC, except for internal battery.
5. Conducted Susceptibility (CS-114) - This test verifies that the unit will safely operate during current fluctuations along its cables. During the exposure the unit is tested while operating on each possible power source that it is configured for, such as 110VAC/60Hz, 110VAC/400Hz, and 28VDC, except for internal rechargeable battery.
SP0200-06-R-8014 Page 38 of 217
6. Conducted Susceptibility (CS-115) - This test verifies that the unit will safely operate during transients in the aircraft's power supply. During the exposure the unit is tested while operating on each possible power source that it is configured for, such as 110VAC/60Hz, 110VAC/400Hz, and 28VDC, except for internal rechargeable battery.
i. Vibration. MIL-STD-810E, Environmental Test Methods and Engineering Guidelines, are followed to test the unit's construction, durability, performance, and the integrity of the mounting device while withstanding random vibration and sinusoidal vibration on the X, Y, and Z axes.
j. Environmental. MIL-STD-810E, the numerical values listed below do not come from any MIL-STD or other source document.
They are modified versions of those in MIL-STDs, and simulated operational conditions. Environmental testing is performed under the following test conditions:
1. Humidity Operation: 94 + 4 percent relative humidity, 85oF + 3.6oF (29.5oC + 2oC) for four hours.
2. Hot Temperature Operation: 120oF + 3.6oF (49oC + 2oC) for two hours.
3. Cold Temperature Operation: 32oF + 7.2oF (0oC+ 4oC) for two hours.
4. Hot Temperature Storage: 140oF + 3.6oF (60oC+ 2oC) for six hours.
5. Cold Temperature Storage: -40oF + 3.6oF (-40oC + 4oC) for six hours.
k. Altitude. MIL-STD-810E, each unit is subjected to reduced atmosphere pressures from 522.7 mmHg, 10,000 ft equivalent in a hypobaric chamber. The exposure time varies with the equipment item under evaluation, but is usually a minimum of 1 hour.
l. Rapid Decompression. Decompressions in flight are uncommon; however, if one were to occur, the unit should not present a hazard to the patient, crew or aircraft operations. Each unit is subjected to a series of rapid decompression (RD) tests, starting at an equivalent pressure altitude of 8,000 ft. with subsequent changes of altitude to 40,000 ft over periods of 60, 7, and 1 second.
m. Airborne Feasibility. Primary objectives of this phase are to identify problems with the unit that could not be evaluated in the lab, assess human factors in the aircraft environment (in accordance with MIL-STD-1472D), assess ease of loading the unit on the aircraft, ensure visibility of visual alarms and audibility of audible alarms, check aircraft interface and unit securing methods, and assess the effect of the combined stresses of flight on the unit.
n. Air Force Aeromedical Test Standards listed above shall be performed at:
Armstrong Laboratory/CFTS…
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