← Back to catalogue

Tourniquets

FDA UDI

Class I (US FDA UDI)

by Typenex Medical, LLC

Identity

Trade Name
Tourniquets FDA UDI
Generic Name
Tourniquet cuff bandage, non-latex FDA UDI
Device Name
Tourniquet 1" x 18", Textured, Flat, Blue FDA UDI
Model / Reference
TQ0103B FDA UDI
Description
Tourniquet 1" x 18", Textured, Flat, Blue FDA UDI

Identifiers

Primary DI / UDI-DI
00810050855570 FDA UDI
FDA Product Code
GAX FDA UDI
GMDN Term
Tourniquet cuff bandage, non-latex 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

Yes

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: Tourniquet cuff bandage, non-latex

Tourniquets by Typenex Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tourniquet cuff bandage, non-latex.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 6d654d53-479c-4695-8433-dfb82a2f2ae8 33 fields · synced May 30, 2026