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Bahadir USA Y105.92M

by Bahadir USA LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB060Y10592M02 UDI-DI Date15 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Bahadir USA
Generic Name
Device sterilization/disinfection container, reusable
Model / Reference
Y105.92M
Description
XXL NON-PERFORATED BOTTOM 770X315X170mm
Primary DI / UDI-DI
B060Y10592M02
510(k) Number
FDA Product Code
KCT
GMDN Term
Device sterilization/disinfection container, reusable
Device Class
Class II
Regulation Number
880.6850
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K131407)

Show all (12)

Other devices from Bahadir USA LLC

See all devices from Bahadir USA LLC →

Properties

  • Lot / Batch Number

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No