MODIFICATION
99 -- Oximeter Simulator
- Notice Date
- 8/3/2010
- Notice Type
- Modification/Amendment
- NAICS
- 423450
— Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers
- Contracting Office
- N62645 Naval Medical Logistics Command 693 Neiman Street Ft. Detrick, MD
- ZIP Code
- 00000
- Solicitation Number
- N6264585017
- Archive Date
- 8/10/2010
- Point of Contact
- Jaime R. Belletto, Phone: 3016193020
- E-Mail Address
-
jaime.belletto@med.navy.mil
(jaime.belletto@med.navy.mil)
- Small Business Set-Aside
- N/A
- Description
- The USNS Mercy has a requirement for an Oximeter Simulator. The following is the essential characterics. Please sumbit information along with quote to jaime.belletto@med.navy.mil. by closing date of July 10th 2010, 3:00 p.m. Essential CharacteristicsA portable, FDA approved Pulse Oximeter Simulator is needed. The simulator shall be battery operated and at minimum operate for 35 hours in continuous use. The unit shall be handheld, portable, and provide SP02 accuracy of +-1 %. The unit shall be capable of detecting heart rate within the selection of 30-200 beats per minute (BPM) with an accuracy of +-1 BPM. The simulator shall accommodate for signal artifacts such as movement. The preset patient types shall cover; normal adult, tachycardia, bradycardia, neonate, and hypoxia patient types. The simulator shall give out an audible alarm for low saturation (SpO2), high/low heart rate (BPM), and low signal amplitude (AMP). The unit shall have an internally loaded R curve adjustment capability for various monitors. The simulator shall support full range of SpO2 technologies including Nellcor and Ohmeda and shall be compatible with a wide range of pulse oximeters. The simulator shall have a membrane/touch pad with a digital screen. The unit shall weigh less than 5 lbs (2.3kgs) and support a Nelcor Port. The unit shall be handheld and the dimensions shall not exceed 7 in x 9 in x 3 in. The unit shall be compliant with CSA/UL, IEC 801-4 Level B, IEC 801-2 Level B, EN 610004-3 Level A, and EN 55022:1994 Class B standards. The voltage requirement is 120V. The system and all of the components, shall be compliant with the Food and Drug Administration (FDA) requirements to market and deliver medical products for use in the United States of America, even should delivery be requested outside of the United States. The claims made for the product shall comply with the regulations of the FDA with respect to products for marketing and delivery of a medical product for use in the United States of America, even should delivery be requested outside of the United States. Technical proposals must include detailed information to enable evaluation on the following seven factors:1) Fit, form, function, conformance to salient characteristics2) Consumable, durable stocked base3) Vendor/OEM support for deployed forces4) Equipment will be piece part supported through useful life of equipment5) Must be able to be shipped OCONUS and supported6) Must supply 2 tech mans and 2 service manuals or CD's7)Provisioned to be secured for sea with a quick release mechanism
- Web Link
-
FBO.gov Permalink
(https://www.fbo.gov/spg/DON/BUMED/N62645/N6264585017/listing.html)
- Record
- SN02227792-W 20100805/100804000215-46b143fd914485c1640d2b308eaf3c29 (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
(may not be valid after Archive Date)
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