← Back to catalogue

Centurion

FDA UDI

Class I (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
Limb tourniquet, manual, single-use FDA UDI
Device Name
LATEX FREE TOURNIQUET SUB PACKED/100 FDA UDI
Model / Reference
LF18S100 FDA UDI
Description
LATEX FREE TOURNIQUET SUB PACKED/100 FDA UDI

Identifiers

Catalog Number
LF18S100 FDA UDI
Primary DI / UDI-DI
20653160162688 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Limb tourniquet, manual, single-use

Centurion by Centurion Medical Products — 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

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

Manufacturer

Sources (1)

  • FDA UDI 8dd8fb2b-1ef0-41fa-8481-b9d093c3f39e 35 fields · synced May 30, 2026