Trinity Sterile, Inc. 10001
Trinity Sterile, Inc. 10001 is a Class I device made by Trinity Sterile, Inc., listed in FDA GUDID since 28 Mar 2023 (UDI-DI 40841767106066), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number40841767106066 | Date28 Mar 2023 | StatusListed |
Official records
- AccessGUDID record 40841767106066
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Trinity Sterile, Inc.
- Generic name
- Limb tourniquet, manual, single-use
- Model / reference
- 10001
- Primary DI / UDI-DI
- 40841767106066
- FDA product code
- GAX
- GMDN term
- Limb tourniquet, manual, single-use
- Device class
- Class I
- Regulation number
- 878.5900
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
Similar devices in this category
Other devices filed under Limb tourniquet, manual, single-use.
- Tender and Tiny Tourniquets 11TA by Small Beginnings, Inc.
- X8T Emergency Tourniquet X8T-E2G X8T-E3G by RCR MEDICAL PRODUCTS LLC
- VYGON 5805.02 00580502 by VYGON
- Tender and Tiny Tourniquets 11TH by Small Beginnings, Inc.
- VYGON 5805.01 00580501 by VYGON
- X8T Tactical Tourniquet X8T-T2G X8T-T3G by RCR MEDICAL PRODUCTS LLC
- Prometheus FullStop Tourniquet - Black PDF180 by SAFEGUARD MEDICAL TECHNOLOGIES LIMITED