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This Combined Synopsis/Solicitation opportunity from Department Of Defense was posted on August 13, 2020. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

Ear, Nose & Throat (ENT) Examination/Treatment Chair for the Landstuhl Regional Medical Center, Germany

Closed
W9114F20Q0019Federal

Contract Overview

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

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General Info

NAICS

339113 - Surgical Appliance and Supplies Manufacturing

Place of Performance

Landstuhl, AE, 66849, DEU

Set-Aside

NONE

Documents

1

W9114F20Q0019+RFQ.pdf

PDF

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Timeline

1 update
PhaseClosed
Posted

Combined Synopsis

Response Deadline

Deadline has passed

Notice updated

Notice details unchanged. Attachments may have changed.

Submission Closed

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Organization & Contact Information

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AgencyDepartment Of Defense → W40M Mrco Europe
Contacts2 people available
OfficeAPO, AE, 09180-0402, USA
Office AddressAPO, AE, 09180-0402, USA
Contacts
Henning Mayer-Goldstein
Richard G. Himebrook

Full Description

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This solicitation is for deliveries of Ear Nose & Throat (ENT) Examination Chairs for the Landstuhl Regional Medical Center in Germany. The contract type will be a Firm Fixed Price Purchase Order as a result of the solicitation. The solicitation is issued for full and open competition. It is incumbent upon interested parties to review this site frequently for any updates/amendments to any and all documents. Purchase Order will be issued using Lowest Price Technically Acceptable (LPTA) evaluation techniques. All vendors must be registered in the System for Award Management (SAM) prior to award, and lack of registration shall make a quotation ineligible for award. Vendors may obtain information on registration and annual confirmation requirements by calling +1 (555) 000-0000 or via Internet at https://www.sam.gov. Technical Factor. The quoter must demonstrate compliance with the requirements in the solicitation by submitting a written quote which addresses compliance with each of the following technical factors: Subfactor 1: The delivered equipment shall be new and not a used or remanufactured product. Subfactor 2: Equipment must possess or meet FDA certification requirements. Subfactor 3: Equipment must have a 12 months warranty or more. Subfactor 4: Equipment must comply with German electrical requirements of 220V/50Hz and have a European two-prong power plug. Subfactor 5: Equipment must meet all salient characteristics. Salient Characteristics of Power ENT Examination/Treatment Chair: Equipment must - be specifically designed for Ear, Nose & Throat (ENT) specialists, - have a light, - have a double articulating headrest, - have armrests that can be dropped during a procedure, - have a foldable footrest, - be electrically powered, - have control buttons on both sides of the chair, - has to have programmable position settings, - have a narrow base footprint which shall not exceed 34 inches x 24 inches, - be able to rotate 360 degree, - be low enough to be low enough for easy patient access (21 from floor or less), - be high enough to accommodate a physician that stands (35 from floor or more), - be able to recline into a flat position, - be able to adjust/tilt the back portion of the chair. (End of Salient Characteristics) Failure to receive an Acceptable rating of any of the above technical evaluation factors / salient characteristics will result in an Unacceptable technical rating unless the error(s), deficiency (ies) or omission (s) can be corrected.

More opportunities from Department Of Defense → W40M Mrco Europe

Same awarding agency

NAICS: 325413
Federal
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The Medical Readiness Contracting Office-Europe is soliciting a Fixed-Price Indefinite Delivery/Indefinite Quantity contract for one automated chemistry analyzer and associated consumables to support the laboratory mission at the U.S. Army Health Clinic in Vicenza, Italy. Under a Cost Per Reportable Result pricing structure, the successful offeror will provide all new equipment, reagents, consumables, controls, and necessary maintenance. The contract includes a two-month phase-in period from January 2, 2026, to February 28, 2026, followed by an ordering period from March 1, 2026, through December 31, 2030. The estimated annual clinical chemistry workload is 42,595 tests. Technical requirements specify that the analyzer must be FDA-approved, capable of measuring analytes from a 300-microliter sample, and equipped with an uninterruptible power supply providing seven minutes of power. The system must have a current Authorization to Operate for interfacing with the Laboratory Information System and comply with the Risk Management Framework for DOD IT. The contractor is responsible for providing initial on-site operator training in English and ensuring all reagents are delivered at the proper storage temperature. Award will be based on the Lowest Price Technically Acceptable evaluation process under Simplified Acquisition Procedures, with the solicitation open for full competition under NAICS code 325413.
In-Vitro Diagnostic Substance Manufacturing

POSTED

12 months ago

DEADLINE

N/A
View Details

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