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Tourniquet System

FDA UDI

Class I (US FDA UDI)

by Anetic Aid USA LLC

Identity

Trade Name
Tourniquet System FDA UDI
Generic Name
Tourniquet cuff, single-use FDA UDI
Model / Reference
Single-use Sterile Tourniquet Cuff - Large Leg - Conical FDA UDI

Identifiers

Catalog Number
40878 FDA UDI
Primary DI / UDI-DI
06975218190352 FDA UDI
FDA Product Code
KCY FDA UDI
GMDN Term
Tourniquet cuff, single-use 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tourniquet cuff, single-use

Tourniquet System by Anetic Aid USA LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tourniquet cuff, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Anetic Aid USA LLC

Sources (1)

  • FDA UDI f0d50afa-01d5-432d-aa63-f17d78e8d1b2 33 fields · synced May 30, 2026