SOLICITATION NOTICE
65 -- Airworthy Certified B. Braun Infusomat 2nd Generation Infusion Pumps
- Notice Date
- 4/6/2020 12:26:22 PM
- Notice Type
- Presolicitation
- NAICS
- 339112
— Surgical and Medical Instrument Manufacturing
- Contracting Office
- NAVAL MEDICAL LOGISTICS COMMAND FORT DETRICK MD 21702-9203 USA
- ZIP Code
- 21702-9203
- Solicitation Number
- N6264520RC6Z006
- Response Due
- 4/21/2020 10:00:00 AM
- Archive Date
- 05/21/2020
- Point of Contact
- Laura A. Lebherz
- E-Mail Address
-
laura.a.lebherz.civ@mail.mil
(laura.a.lebherz.civ@mail.mil)
- Description
- The Naval Medical Logistics Command (NMLC) intends to negotiate on a sole source basis (in accordance with FAR Part 13.501(a)).� The proposed source is Golden Max LLC DBA Optimal Government Services, 12701 Directors Drive, Stafford TX 774777. The Naval Medical Logistics Command (NMLC) has a requirement for four hundred and fourteen (414) sets of Airworthy Certified B. Braun Infusomat 2nd Generation Infusion Pumps and accessories for twenty two (22) U.S. Navy ships � USS Carl Vinson (CVN70), USS Theodore Roosevelt (CVN71), USS Dwight Eisenhower (CVN69), USS Blue Ridge (LCC19), USS America (LHA6), USS Essex (LHD2), USS Boxer (LHD4), USS Bonhomme Richard (LHD6), USS Makin Island (LHD8), USS Wasp (LHD1), USS New Orleans (LPD18), USS Green Bay (LPD20), USS San Diego (LPD22), USS Anchorage (LPD23), USS Somerset (LPD25), USS John P. Murtha (LPD26), USS Portland (LPD27), USS Germantown (LSD42), USS Rushmore (LSD47), USS Ashland (LSD48), USS Harpers Ferry (LSD49), and USS Pearl Harbor (LSD52). This procurement includes the infusion pump, power supply, clinical support, drug library, and accessories. � Vendor shall be an Original Equipment Manufacturer (OEM) authorized dealer, authorized distributor, or authorized reseller for the proposed equipment, such that OEM warranty and service are provided and maintained by the OEM. All software licensing, warranty, and service associated with the equipment shall be in accordance with the OEM terms and conditions. The equipment, including claims made for the product, shall be compliant with Food and Drug Administration (FDA) regulations, with respect to marketing and delivering medical products for use in the United States of America. These requirements shall apply even if delivery is requested outside of the United States of America. The equipment shall be installed in compliance with Occupational Safety and Health Administration (OSHA) requirements. The vendor shall provide infusion pumps, power supply, clinical support, drug library, and accessories. The vendor shall be responsible for conducting initial calibration, and operational and performance tests for the Infusion Pumps.
- Web Link
-
SAM.gov Permalink
(https://beta.sam.gov/opp/2aea9f0e64db4978bb803ab2edefd5df/view)
- Record
- SN05611793-F 20200408/200406230148 (samdaily.us)
- Source
-
SAM.gov Link to This Notice
(may not be valid after Archive Date)
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