SOURCES SOUGHT
65 -- Single and Multi-Channel Infusion Pumps - Request for Information Infusion Pumps
- Notice Date
- 10/27/2011
- Notice Type
- Sources Sought
- NAICS
- 339112
— Surgical and Medical Instrument Manufacturing
- Contracting Office
- Defense Logistics Agency, DLA Acquisition Locations, DLA Troop Support - Medical, 700 Robbins Avenue, Philadelphia, Pennsylvania, 19111-5096, United States
- ZIP Code
- 19111-5096
- Solicitation Number
- SPM2D1-12-RFI-8001
- Point of Contact
- Valerie Panacio, Phone: 215-737-2470
- E-Mail Address
-
Valerie.Panacio@dla.mil
(Valerie.Panacio@dla.mil)
- Small Business Set-Aside
- N/A
- Description
- Essential Characteristcs Checklist Single and Multi-Channel Infusion Pumps ESSENTIAL CHARACTERISTICS (ECs): The essential characteristics of the Single Channel, Stackable Individual, or Multi-Channel Infusion Pump (MCIP) device are as follows: Key Performance Parameters are identified as "(KPP)" •EC 1. The pump shall be Food and Drug Administration (FDA) cleared and compliant with current versions of the Association for the Advancement of Medical Instrumentation (AAMI) infusion pump standards (ANSI/AAMI ID26) (KPP). •EC 2. The pump shall be a portable, single channel (stackable or unstackable), or multi-channel volumetric intravenous infusion pump that operates on 110-120 VAC, 60 Hz and 220-240 VAC, 50 Hz as well as incorporated rechargeable battery power (KPP). Automatic switching between these power sources is strongly preferred. •EC 3. While battery operated, pump shall be capable of at least 4 hours of operation at 125 ml/hr on all channels. Power cord and 12 VDC adapter cigarette lighter type are to be included to provide additional power capability. The internal battery shall automatically charge while the pump is operating at 100-240 VAC, 50/60 Hz. (KPP) •EC 4. The pump shall have a Dose Error Reduction System (DERS) and allow for digitally displayed medication identification and dose calculation rates with upgradeable software. (KPP) Shall be easy to set-up, program, and use, with displays that are easily visible in both low-light and outdoor settings. Pump device will have over-ride capability for drug calculation if deemed necessary and include dosage and rate error notices. •EC 5. The pump shall incorporate free-flow protection. (KPP) •EC 6. The pump shall maintain an accurate flow rate to within 5% of the rate set. •EC 7. The pump shall deliver a pre‑selected administration volume within the range of 1 to 999 ml and provide a selectable infusion range which includes 1 to 999 ml/hr in increments no larger than 1 ml. •EC 8. The pump shall revert to a keep vein open (KVO) rate once the programmed volume is delivered. •EC 9. The pump shall be provided with a suitable bracket to enable attachment to a standard IV pole. • EC 10. The pump mechanism shall be capable of accepting a variety of commercially available standard in travenous administration sets. If proprietary tubing is used, so state and list recommended standard or common tubing types/sets by part number and description.
- Web Link
-
FBO.gov Permalink
(https://www.fbo.gov/spg/DLA/J3/DSCP-M/SPM2D1-12-RFI-8001/listing.html)
- Record
- SN02614165-W 20111029/111027234618-51b98a54427454c83dbe2cc7e2ed211d (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
(may not be valid after Archive Date)
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