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Ostoh OSV001

by Ostoh, LLC

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860010269800 UDI-DI Date16 Dec 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ostoh
Generic Name
Ostomy bag pressure release valve
Model / Ref / Catalog
OSV001
Primary DI / UDI-DI
00860010269800
FDA Product Code
EZS
GMDN Term
Ostomy bag pressure release valve
Device Class
Class I
Regulation Number
876.5900
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ostomy bag pressure release valve

Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Manufacturing Date: No