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This Sources Sought opportunity was posted on October 27, 2011. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Single and Multi-Channel Infusion Pumps

Closed
SPM2D1-12-RFI-8001Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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General Info

Agency

N/A

NAICS

339112 - Surgical and Medical Instrument Manufacturing

Place of Performance

Not specified

Set-Aside

NONE

Documents

0

No documents available

Documents will appear here when they are available.

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Timeline

PhaseClosed
Posted

Sources Sought

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyN/A
Contacts1 person available
OfficeN/A
Organization / Agency
N/A
Office AddressN/A
Contacts
Valerie PanacioContract Specialist

Full Description

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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 intravenous administration sets. If proprietary tubing is used, so state and list recommended standard or common tubing types/sets by part number and description.

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