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MedSource Tourniquet MS-17301-SM

by Medsource International LLC

MedSource Tourniquet MS-17301-SM (Not Applicable) is a Class I device made by Medsource International LLC, listed in FDA GUDID since 10 May 2021 (UDI-DI 00816703025246), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816703025246 UDI-DI Date10 May 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
MedSource Tourniquet
Generic name
Limb tourniquet, manual, single-use
Model / Ref / Catalog
MS-17301-SM, Not Applicable
Primary DI / UDI-DI
00816703025246
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

Related devices

Category: Limb tourniquet, manual, single-use

Other devices from Medsource International LLC

See all devices from Medsource International LLC →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)