MediChoice

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name: MediChoice FDA UDI
Generic Name: Limb tourniquet, manual, single-use FDA UDI
Device Name: Tourniquet Perforated Roll Single-patient Use Polyisoprene 1inchx18inches Blue Textured Not Made With Natural Rubber Latex MediChoice FDA UDI
Model / Reference: TRN1191B FDA UDI
Description: Tourniquet Perforated Roll Single-patient Use Polyisoprene 1inchx18inches Blue Textured Not Made With Natural Rubber Latex MediChoice FDA UDI

Identifiers

Primary DI / UDI-DI: 30885632128220 FDA UDI
FDA Product Code: GAX FDA UDI
GMDN Term: Limb tourniquet, manual, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Limb tourniquet, manual, single-use

MediChoice by Owens & Minor Distribution, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Owens & Minor Distribution, Inc.

Sources (1)

FDA UDI 48738b60-3e3d-459c-938d-9c67157aee21 33 fields · synced Jun 8, 2026