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Stethoscopes

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StethoscopesFederal

Contract Overview

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

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The Defense Health Agency Medical Logistics Division Medical Materiel Enterprise Standardization Office is conducting market research to establish a Qualified Supplier List for the standardization of stethoscopes. This Request for Information is intended to gather technical data and supporting documentation from industry partners to assist in acquisition planning and the definition of future requirements. The scope of the product line includes single-head, dual-head, adult, pediatric, infant, and cardiology stethoscopes with various lumen and tubing configurations, provided they are not made with natural rubber latex and are not disposable. Interested vendors must submit a response package via the RFI Vendor Response Worksheet, including company identification, CAGE code, country of origin, and detailed technical specifications. The government is specifically seeking information regarding warranty terms, replacement part availability, recall history, and any emerging technologies. All submitted information will be treated as unrestricted and may be incorporated into future acquisition documents. This notice serves as an announcement that the QSL release has been issued, with all solicitation details available electronically on the System for Award Management website.

General Info

DHA seeks qualified suppliers for standardized, non-latex stethoscopes through a market research RFI.

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

Medical Materiel Enterprise Standardization Offices (MMESO) Northern Regional Medical Command HQ ATTN: ACSLA (MCAT-LA) Buildin, Fort Belvoir, VA, 22060, USA

Set-Aside

NONE

Documents

1

QSL RFI Vendor Response Worksheet - Stethoscopes

XLSX, High priority: read this first2 pages · rfi
High

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Timeline

3 updates
Posted

Presolicitation

Notice updated

The notice description changed.

Notice updated

Notice type changed from Presolicitation to Special Notice. Response deadline added: Jul 17, 2019. The notice description changed. The point of contact changed.

Notice updated

The response deadline was removed. The notice description changed.

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Organization & Contact Information

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AgencyDepartment Of Defense → DLA Troop Support
Contacts1 person available
OfficePHILADELPHIA, PA, 19111, USA
Office AddressPHILADELPHIA, PA, 19111, USA

Full Description

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The purpose of this modification is to inform qualified entities interested in providing these services that the release of the QSL Announcement has been issued. All solicitation information is available electronically on the System for Award Management (SAM) website. REQUEST FOR INFORMATION (RFI) Stethoscopes 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 Stethoscopes. 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 Stethoscopes. 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 provide 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 This Stethoscope product line could include, but is not limited to: single-head, dual-head, adult, pediatric infant, and cardiology stethoscopes with both single and double lumen; bendable tubing; flexible binaural; ear tips; a non-chill diaphragm ring; with components not made with natural rubber latex. This product line does not include disposable stethoscopes. 3.0 Characteristics/Specifications Feedback Requested: Vendors are requested to provide information about their Stethoscopes (See Vendor Response Worksheet). 3.1 What is the Country of Origin of your Stethoscope products? 3.2 What are the technical specifications used to differentiate between your cardiology, general, pediatric and infant Stethoscopes? (I.e. single lumen, double lumen, dual tubing or single tubing, diaphragm, bell and, length, etc.) 3.3 Do your Stethoscopes come with a warranty? If so, how long is the warranty? 3.4 Which replacement parts are available for the Stethoscopes? How long will the parts be available after purchase? 4.0 Additional Feedback Please complete the attached RFI Vendor Response Worksheet with indicated information about your Stethoscopes. 4.1 Have your Stethoscopes been subject to any recalls? If so, what corrective actions and/or product modifications have been made in response to the recalls? 4.2 Do you have any emerging technology for Stethoscopes that you would like to share? 4.3 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. 7.0 Points of Contact (POCs): Vivian Alexander, MMESO North Team Leader, +1 (555) 000-0000, contact@example.gov and Greg Morrison, MMESO North Clinical Analyst, +1 (555) 000-0000, contact@example.gov. The purpose of this modification is to inform qualified entities interested in providing these services that the release of the QSL Announcement has been issued. All solicitation information is available electronically on the System for Award Management (SAM) website.

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