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Bahadir USA Y600.02

by Bahadir USA LLC

Bahadir USA Y600.02 is a Class II device made by Bahadir USA LLC, cleared under FDA 510(k) K131407 on 12 Aug 2014 and listed in FDA GUDID since 17 Feb 2017 (UDI-DI B060Y600021), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K131407

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB060Y600021 UDI-DI Date17 Feb 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated NumberK131407 Date12 Aug 2014DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K131407 decided 12 Aug 2014 Active
  • FDA GUDID UDI-DI B060Y600021 listed 17 Feb 2017 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K131407
  2. Listed FDA GUDID B060Y600021

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Bahadir USA
Generic name
Instrument tray, reusable
Model / reference
Y600.02
Description
IMPLANT SCOPE CONTAINER LID 450x70x70MM
Primary DI / UDI-DI
B060Y600021
510(k) Number
FDA product code
KCT
GMDN term
Instrument tray, reusable
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Instrument tray, reusable

Cleared under the same submission (K131407)

and 8 more cleared under K131407

Similar devices in this category

Other devices filed under Instrument tray, reusable.

Other devices from Bahadir USA LLC

See all devices from Bahadir USA LLC →

Properties

  • Lot / batch number
Other properties (14, all answered No)