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Single Use Tourniquets

FDA UDI

Class I (US FDA UDI)

by Timesco Healthcare Limited

Identity

Trade Name
Single Use Tourniquets FDA UDI
Generic Name
Limb tourniquet, manual, single-use FDA UDI
Device Name
Button Tourniquet Single Use (Pack 100) FDA UDI
Model / Reference
D80.150 FDA UDI
Description
Button Tourniquet Single Use (Pack 100) FDA UDI

Identifiers

Primary DI / UDI-DI
05055382858263 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

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

Yes

FDA UDI

Category: Limb tourniquet, manual, single-use

Single Use Tourniquets by Timesco Healthcare Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Limb tourniquet, manual, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fa281551-0d9c-4ec6-a180-48470b28661a 34 fields · synced May 30, 2026