MedSource Tourniquet MS-17315
by Medsource International LLC
MedSource Tourniquet MS-17315 (Not Applicable) is a Class I device made by Medsource International LLC, listed in FDA GUDID since 10 May 2021 (UDI-DI 00816703025376), registry data as of 22 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 | Number00816703025376 | Date10 May 2021 | StatusListed |
Official records
- AccessGUDID record 00816703025376
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- MedSource Tourniquet
- Generic name
- Limb tourniquet, manual, single-use
- Model / Ref / Catalog
- MS-17315, Not Applicable
- Description
- 1"x18" Light Blue Rolled Tourniquet
- Primary DI / UDI-DI
- 00816703025376
- 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
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