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CONTROL, GLUCOSE

Active
SPE2DS-27-T-0564Federal

Contract Overview

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

General Info

NAICS

325413 - In-Vitro Diagnostic Substance Manufacturing

Place of Performance

4101 WASHINGTON AVE BLDG 2, NEWPORT NEWS, VA, 23607-2787, USA

Set-Aside

NONE

Documents

1

SPE2DS-27-T-0564.pdf

PDF

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Timeline

PhaseSolicitation
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Solicitation

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN MD SURG FSF
Contacts1 person available
OfficeUSA
Office AddressUSA
Contacts

Full Description

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CONTROL,GLUCOSE
CONTROL,GLUCOSE
PRODIGY BLOOD GLUCOSE CONTROL SOLUTION HIGH LEVEL 2; TO ENSURE ACCURATE
BLOOD GLUCOSE TESTING WITH THE PRODIGY BLOOD GLUCOSE MONITORING SYSTEMS
UNIT ISSUE: EACH (4ML SOLUTION)
..
RA001: THIS DOCUMENT INCORPORATES TECHNICAL AND/OR QUALITY REQUIREMENTS
(IDENTIFIED BY AN 'R' OR AN 'I' NUMBER) SET FORTH IN FULL TEXT IN THE
DLA MASTER LIST OF TECHNICAL AND QUALITY REQUIREMENTS FOUND ON THE WEB
AT:
http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx http://www.dla.mil/HQ/Acquisition/Offers/eProcurement.aspx
FOR SIMPLIFIED ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE SOLICITATION ISSUE DATE OR THE AWARD DATE CONTROLS. FOR LARGE ACQUISITIONS, THE REVISION OF THE MASTER IN EFFECT ON THE RFP ISSUE DATE APPLIES UNLESS A SOLICITATION AMENDMENT INCORPORATES A FOLLOW-ON REVISION, IN WHICH CASE THE AMENDMENT DATE CONTROLS.
..
RD003, COVERED DEFENSE INFORMATION POTENTIALLY APPLIES
..
RP001: DLA PACKAGING REQUIREMENTS FOR PROCUREMENT
..
RQ011: REMOVAL OF GOVERNMENT IDENTIFICATION FROM NON-ACCEPTED SUPPLIES
..
APPLICABLE TO ALL MEDICAL ACQUISITIONS:
PACKAGING AND PACKING SHALL BE COMMERCIAL AS
SPECIFIED IN THE PROCUREMENT DOCUMENT.
EACH COMPLETE UNIT SHALL BE PROPERLY PACKAGED
IN A SUITABLE SEALED UNIT CONTAINER CAPABLE
OF PROTECTING THE CONTENTS FROM DAMAGE AND/OR
BREAKAGE.
UNITS SHALL BE PACKED IN SUITABLE COMMERCIAL
EXTERIOR (SHIPPING) CONTAINERS (EXPORT WHEN
NECESSARY) WHICH SHALL INSURE ACCEPTANCE AND
SAFE DELIVERY BY COMMON OR OTHER CARRIER, AT
THE LOWEST RATE, TO POINT OF DELIVERY CALLED
FOR IN THE CONTRACT OR ORDER.
MATERIAL MUST BE MARKED IAW MEDICAL MARKING
STANDARD NO. 1. THIS SUPERCEDES ALL REFERENCES
TO MIL-STD-129.
COPIES OF MEDICAL MARKING STANDARD NO. 1
(MMS NO. 1) MAY BE OBTAINED BY CONTACTING DLA
TROOP SUPPORT VIA EMAIL TO fssb@dla.mil. MMS NO. 1 IS ALSO AVAILABLE ONLINE AT: https://www.dla.mil/Logistics-Operations/Packaging/
.. RS016: Shelf-life requirement RS001 for a TYPE I (CODE M) item with a shelf life of 24 months (non-extendable) applies to this item.
SPE2DS-27-T-0564
SECTION B
SHALL HAVE A SHELF LIFE OF 24 MONTHS.
NOT MORE THAN 4 MONTHS SHALL HAVE ELAPSED FROM
DATE OF MANUFACTURE TO DATE OF DELIVERY TO THE
GOVERNMENT.
.
SHELF LIFE MARKINGS SHALL BE IN ACCORDANCE WITH
THE LATEST REVISION OF MMS1C.
. ALL LABELS SHALL INCLUDE:
DATE OF MANUFACTURE, EXPIRATION, OR RETEST DATE
CONTRACT NUMBER/LOT NUMBER.
..
MUST BE STORED AT 36° TO 86°FAHRENHEIT (2° TO 30° CELSIUS), DO NOT
FREEZE
..
BIDDER: PLEASE SPECIFY SOURCE AND PART
NUMBER BEING SUPPLIED.
ADEQUATE DATA FOR THE NSN/Part Number: 6550-01-698-2104 Quantity: 1 EA Purchase Request: 7018667584QTY: 1 Delivery: 5 days ADO

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4 days ago

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Solicitation SPE2DS-27-T-0361, issued by the DLA Troop Support Medical Supply Chain, is for the procurement of one kit of BioFire RP2.1/RP2.1Plus Control Panels (NSN 6550-01-690-4435). These panels are intended for in vitro use as quality controls to monitor the detection and identification of respiratory pathogens using the FilmArray RP2.1 Panel Assay on a FilmArray instrument. Each kit contains 12 tubes of 300uL synthetic nucleic acid, consisting of six positive and six negative controls, providing enough reagent for six quality control runs. The product requires strict frozen storage between -25 and -15 degrees Celsius. The contract mandates a delivery timeline of 83 days after receipt of order, with destination inspection and acceptance. Key quality and technical requirements are governed by the DLA Master List, and packaging must be commercial and compliant with MIL-STD-2073-1E and RP001. Marking must adhere to Medical Marking Standard No. 1 and MIL-STD-129. The item has a non-extendable shelf life of 18 months, with a requirement that no more than two months elapse between the date of manufacture and delivery to the government. Administrative requirements include electronic submission of payment requests via the Wide Area Workflow system and compliance with various FAR and DFARS clauses regarding cybersecurity, domestic sourcing, and the prohibition of covered telecommunications equipment.
MEDICAL SUPPLY CHAIN MD SURG FSF

POSTED

8 days ago

DEADLINE

in about 5 hours
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