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This Government Contract opportunity was posted on April 9, 2019. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

RFI_Syringes_With_Safety_Needles

Closed
RFI_Syringes_With_Safety_NeedlesFederal

Contract Overview

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The Defense Health Agency is seeking input from industry to develop a Qualified Supplier List for standardizing syringes with safety needles through a market research initiative. This Request for Information is not a solicitation for quotes or proposals but rather a tool to gather technical details, capabilities, and innovations from vendors to inform future acquisition planning. Respondents are required to complete a Vendor Response Worksheet addressing key specifications including compliance with Trade Agreements Act requirements, whether safety needles are detachable or permanently attached, compatibility with needleless systems, use of color coding tied to industry standards, and whether needles are made from medical grade steel. All products must be single use, sterile, plastic, nonlatex, and available in varying capacities, lengths, and gauges. The government will use the submitted data to shape future procurement requirements and may incorporate all provided information into future contracts without attribution or vendor approval. Vendors must submit responses by the deadline, including their company name, address, point of contact details with phone and email, and their Commercial and Government Entity code. Additional feedback on emerging technologies or any other relevant information is encouraged but voluntary. The response must be submitted via the designated worksheet and any submitted material will be treated as unrestricted government information. The government assumes no liability for costs incurred by vendors in preparing submissions. Points of contact for questions are Vivian Alexander and Harris Satari of the Medical Materiel Enterprise Standardization Office, and all responses should be directed to the specified email addresses. The place of performance for this initiative is Fort Belvoir, Virginia.

General Info

Defense Health Agency seeks industry input on safety syringe specs for future procurement, requiring TAA compliance and standardized features.

Agency

N/A

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

Medical Materiel Enterprise Standardization Offices Northern Regional Medical Command HQ ATTN: ACSLA (MCAT-LA) Building 1221 2, FORT BELVOIR, VA, 22060, USA

Set-Aside

NONE

Documents

0

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Timeline

PhaseClosed
Posted

special-notice

Response Deadline

Deadline has passed

Submission Closed

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Organization & Contact Information

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AgencyN/A
Contacts2 people available
OfficeN/A
Organization / Agency
N/A
Office AddressN/A
Contacts
Ms Vivian AlexanderMMESO North Team Leader
Mr. Harris SatariMMESO North Clinical Analyst

Full Description

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REQUEST FOR INFORMATION (RFI) Syringes with Safety Needles 1.0 Introduction 1.1 General. The purpose of this request is to obtain information from industry to support the government's intent to establish a Qualified Supplier List (QSL) for the standardization of Syringes with Safety Needles. This RFI is an invitation to submit to the Defense Health Agency (DHA) Medical Logistics (MEDLOG) Division Medical Materiel Enterprise Standardization Office (MMESO) the following: technical information and all related supporting documentation for Syringes with Safety Needles. This request is a market research effort undertaken by the government which will be used for information gathering purposes. The information received may be used for Acquisition Planning purposes and may help define future requirements for the subject item(s). This is not a request for quote or proposal. 1.2 RFI Submission Package. Vendors are requested to provide responses to this RFI via the RFI Vendor Response Worksheet. Complete answers and provided supporting documentation with response. Responses for each salient characteristic should be in the form of yes, no, or descriptive explanation. Additional comments may be provided for all responses. 2.0 Scope Examples of items for this product line could include but are not limited to: single use, sterile, plastic hypodermic syringes with safety needles, with graduation markings and a sharps safety feature. These products will be available in various syringe volume capacities, needle lengths, and needle gauges. All products are not made with natural rubber latex. 3.0 Characteristics/Specifications Feedback Requested: Vendors are requested to provide information about their Syringes with Safety Needles (See Vendor Response Worksheet). 3.1 Are your Syringes with Safety Needles manufactured in a TAA compliant country? Please supply the country of origin. 3.2 Are your Safety Needles detachable or permanently attached to the syringe? 3.3 Can your Syringes with Safety Needles be used with needleless systems? 3.4 Are your Syringes with Safety Needles offered with color coding? Which industry standard is your color code system based on? 3.5 Are your Safety Needles made of medical grade steel material? 4.0 Additional Feedback Please complete the attached RFI Vendor Response Worksheet with indicated information about your Syringes with Safety Needles. 4.1 Do you have any emerging technology for Syringes with Safety Needles that you would like to share? 4.2 Please provide any additional information including relative topics outside of the specific information requested which you consider relevant. Any information provided in response to this RFI will be considered and treated as unrestricted information which can be used by the Government in any future planning or acquisitions. All information, comments, and suggestions may be incorporated into future acquisition documents, without identifying the source or obtaining prior approval from the source. 5.0 Liability The Government shall not be responsible or liable for any costs incurred by any party in the preparation and submission of any response to this RFI. 6.0 RFI Responses The vendors' responses shall include all detailed information requested in the RFI Vendor Response Worksheet and shall also include: (1) Company name and address; (2) Company POC (Name and Phone Number, Fax Number, and E-mail address); and (3) Commercial and Government Entity (CAGE) Code. Points of Contact (POCs): Vivian Alexander, MMESO North Team Leader, +1 (555) 000-0000, contact@example.gov and Harris Satari, MMESO North Clinical Analyst, +1 (555) 000-0000, contact@example.gov.

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