This Solicitation opportunity from Department Of Defense was posted on April 16, 2021. The submission period has ended. Browse the details below for market research, or find similar active opportunities.

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Ophthalmoscope, scanning laser

Closed

N6264521Q0022Federal

Submission Closed04/17/2021, 02:00:00 PM UTC

Contract Overview

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

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NAICS: 339112

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Supply of Safety Hypodermic Syringes and NeedlesThis subcontract, managed by the Department of Defense Medical Supply Chain, involves the provision of sterile, disposable, non-toxic, and non-pyrogenic safety hypodermic syringes and needles for prime contractors on DLA supply contracts. The required equipment consists of 3ML capacity syringes equipped with 20Gage needles and a depressing plunger mechanism that automatically retracts the needle into the barrel for safety. All units must be delivered in packages of 100 and strictly adhere to FDA Regulation 880.5860 Class II and MIL-STD-2073-1E standards. The opportunity is categorized under NAICS code 339112, with the place of performance located in Williamsburg, Virginia. Interested parties should note that the solicitation was posted on October 19, 2026, with a response deadline set for October 26, 2026.

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Supply of Obstetrical Field Medical SetsThis subcontract involves the procurement of complete, ready-to-use Obstetrical Field Medical Supply Sets (NSN 013692830) for prime contractors supporting Department of Defense supply contracts. The selected provider is responsible for sourcing and kitting all necessary medical instruments and supplies, ensuring that every component adheres to FDA regulations for regulated drugs or devices. Additionally, all materials must be marked in strict accordance with Medical Marking Standard No. 1. Managed by the Medical Supply Chain MD Surg FSF, the contract falls under NAICS code 339112. The performance of the contract is designated for FPO 09591. Interested parties must adhere to the response deadline of October 26, 2026, to be considered for this requirement.

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MEDICAL SUPPLY CHAIIN FSH

POSTED

1 day ago

DEADLINE

in 6 days

General Info

Agency

Department Of Defense → Naval Medical Logistics Command

Contract Value

$82,777.28

NAICS

339112 - Surgical and Medical Instrument Manufacturing

Place of Performance

MD, JPN

Set-Aside

NONE

Awardee

MELLING LLC

Award Issued Date

05/12/2021, 12:00:00 AM UTC

Documents

DHA+Cyber+Logistics+Center+of+Excellence.pdf

Medical+Device+Risk+Assessment+%28MDRA%29+Form.docx

N6264521Q0022.docx

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Timeline

PhaseClosed

PostedApr 16

Solicitation

Response DeadlineApr 17

Deadline has passed

Submission Closed

04/17/2021, 02:00:00 PM UTC

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Organization & Contact Information

AgencyDepartment Of Defense → Naval Medical Logistics Command

Contacts1 person available

OfficeFORT DETRICK, MD, 21702-9203, USA

Organization / AgencyDepartment Of Defense → Naval Medical Logistics Command

Office AddressFORT DETRICK, MD, 21702-9203, USA

Contacts

Gerrie M. Johnson

contact@example.gov

Full Description

The Naval Medical Logistics Command (NMLC) intends to negotiate on a sole source basis (FAR 13.106-1(b)(1)), soliciting from a single source. The proposed source is Melling, LLC (dba MellingMedical), 658 South Columbus Street, Alexandra, VA 22314. United States Naval Hospital (USNH) Yokosuka has a requirement for one (1) ophthalmoscope, scanning laser [18-190]. The ophthalmoscope shall be able to scan the retina to assess retinal health of adult eyes. The ophthalmoscope shall be able to complete a retinal scan of the eye through a non-mydriatic, non-dilated pupil in less than one minute. The unit shall be capable of scanning a non-dilated pupil with a minimum diameter of 2 mm. The ophthalmoscope shall be capable of scanning a minimum of 200 degrees of the retina in a single panoramic capture. The unit shall be capable of performing iris detection. The ophthalmoscope shall be capable of various wavelengths for different visual depths in order to assess retinal health. The unit shall be capable of viewing the sensory retina to the retinal pigment epithelial (RPE) at a 532 nm wavelength. The unit shall be capable of viewing a deeper depth at 635 nm wavelength that views the RPE to the Choroid. The unit shall be capable of viewing the eye structures at these specific wavelengths to characterize degeneration, diseases, and deterioration to the retina. The unit shall be capable of various procedures including, but not limited to, imaging in color, red-free, and autofluorescence. The electrical requirement for the system is 120 VAC, 60 Hz. The unit shall operate on a DOD supported operating system (OS). The vendor shall provide two (2) operators manuals and two (2) service manuals, each in English. The instrument shall support the Integrating the Healthcare Enterprise (IHE) Eye Care Workflow Integration Profile as an Acquisition Modality Actor with the Patient Instructions Option. The instrument shall support the IHE Eye Care Workflow Integration Profile as an Acquisition Modality with the Relative Image Position Coding Option. The instrument shall send DICOM images to the Eye Care PACS. The instrument DICOM shall not be proprietary. Vendor shall be an Original Equipment Manufacturer (OEM) authorized dealer, authorized distributor or authorized reseller for the proposed equipment/system, such that OEM warranty and service are provided and maintained by the OEM. All software licensing, warranty and service associated with the equipment/system shall be in accordance with the OEM terms and conditions. The systems shall be compliant with the Food and Drug Administration (FDA) requirements to market and deliver medical products for use in the United States of America, even should delivery be requested outside of the United States. The claims made for the product shall comply with the regulations of the FDA, with respect to products for marketing and delivery of a medical product for use in the United States of America, even should delivery be requested outside of the United States. The system shall be installed in compliance with OSHA requirements. Upon delivery, the vendor shall be responsible for uncrating the unit/system, transporting it through the facility to the location of intended use for installation, and removing all trash created in this process. If interim storage is required, the vendor shall make arrangements for the storage.

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