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Medi-First Tourniquet

FDA UDI

Class I (US FDA UDI)

by Medique Products

Identity

Trade Name
Medi-First Tourniquet FDA UDI
Generic Name
Limb tourniquet, manual, reusable FDA UDI
Device Name
A device consisting of a strap intended to be wrapped around a patient's limb and tightened to reduce circulation. FDA UDI
Model / Reference
66002 FDA UDI
Description
A device consisting of a strap intended to be wrapped around a patient's limb and tightened to reduce circulation. FDA UDI

Identifiers

Catalog Number
66002 FDA UDI
Primary DI / UDI-DI
00347682660024 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Limb tourniquet, manual, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Limb tourniquet, manual, reusable

Medi-First Tourniquet by Medique Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Limb tourniquet, manual, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medique Products

Sources (1)

  • FDA UDI 3d5bddea-be28-436a-a93b-96e0fc772dad 35 fields · synced May 30, 2026