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The Quick-T tourniquet

FDA UDI

Class I (US FDA UDI)

by First Care Products Ltd

Identity

Trade Name
The Quick-T tourniquet FDA UDI
Generic Name
Arterial tourniquet, pneumatic FDA UDI
Device Name
The Quick-T tourniquet is a pneumatic, single-use, non-sterile device, which applies preset pressure to stop life-threatening bleeding. FDA UDI
Model / Reference
Quick-T FDA UDI
Description
The Quick-T tourniquet is a pneumatic, single-use, non-sterile device, which applies preset pressure to stop life-threatening bleeding. FDA UDI

Identifiers

Primary DI / UDI-DI
07290017050485 FDA UDI
FDA Product Code
QGX FDA UDI
GMDN Term
Arterial tourniquet, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5910 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

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Arterial tourniquet, pneumatic

The Quick-T tourniquet by First Care Products Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arterial tourniquet, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
First Care Products Ltd

Sources (1)

  • FDA UDI ed505d5d-a76f-4a19-9a8d-6faa9d1d870d 33 fields · synced Jun 1, 2026