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Supply Line International Medical, LLC

US

Last updated May 30, 2026

What Supply Line International Medical, LLC makes

The company manufactures single-use medical syringes, including hypodermic needles, safety-needle medication cartridges, and metered-delivery hypodermic syringes, as well as general-purpose syringe/needle combinations. It also produces non-sterile non-woven gauze pads and single-use medical equipment handle covers. Medication transfer needles without filters or vents are part of its product line.

These devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Supply Line International Medical, LLC primarily manufacture?

Supply Line International Medical, LLC specializes in single-use medical devices, including hypodermic needles, medication cartridge syringes with safety needles, metered-delivery hypodermic syringes, and general-purpose syringe/needle combinations. They also produce non-sterile non-woven gauze pads and single-use medical equipment handle covers, as well as medication transfer needles without filters or vents. These products are designed for clinical and procedural use.

Where is Supply Line International Medical, LLC based?

The company is headquartered in the United States. This location is relevant for regulatory compliance, manufacturing standards, and distribution networks within North America and potentially beyond.

Which regulatory registries or databases list Supply Line International Medical, LLC’s devices?

The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices for regulatory, traceability, and compliance purposes, ensuring transparency in the supply chain.

How are Supply Line International Medical, LLC’s devices classified under FDA regulations?

The company’s products fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. Classification depends on factors like intended use, potential harm, and design complexity.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
844-239-4058
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
079241502

Catalogue (70)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Doctors Choice SY0325105N1
FDA UDI
Class IIActive
Physicians Choice DCC-02
FDA UDI
Class IActive
Doctors Choice SN251506
FDA UDI
Class IIActive
Doctors Choice SYS0106
FDA UDI
Class IIActive
Doctors Choice SY0325625N1
FDA UDI
Class IIActive
Doctors Choice SY0318105N1
FDA UDI
Class IIActive
Doctors Choice SN2525
FDA UDI
Class IIActive
Doctors Choice SY03LL1
FDA UDI
Class IIActive
Doctors Choice SY0323625N1
FDA UDI
Class IIActive
Doctors Choice SND25G0102
FDA UDI
Class IIActive
Doctors Choice SY01LL1
FDA UDI
Class IIActive
Doctors Choice S323625SN1
FDA UDI
Class IIActive
Doctors Choice N27151
FDA UDI
Class IIActive
Doctors Choice SLL32538SN
FDA UDI
Class IIActive
Doctors Choice SN250106
FDA UDI
Class IIActive
Doctors Choice SYSR03251502
FDA UDI
Class IIActive
Doctors Choice SY032510N1
FDA UDI
Class IIActive
Doctors Choice BN18101
FDA UDI
Class IIActive
Doctors Choice SND25G11
FDA UDI
Class IIActive
Doctors Choice SYS01250105
FDA UDI
Class IIActive

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