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Trinity Sterile, Inc.

FDA UDI

Class I (US FDA UDI)

by Trinity Sterile, Inc.

Identity

Trade Name
Trinity Sterile, Inc. FDA UDI
Generic Name
Limb tourniquet, manual, single-use FDA UDI
Device Name
TOURN 1X18 FLAT GREEN FDA UDI
Model / Reference
10086 FDA UDI
Description
TOURN 1X18 FLAT GREEN FDA UDI

Identifiers

Primary DI / UDI-DI
40841767106233 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

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Limb tourniquet, manual, single-use

Trinity Sterile, Inc. by Trinity Sterile, Inc. — 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 8f56834e-6eb1-4b94-b1ad-8090bd619444 33 fields · synced May 30, 2026