Bahadir USA Y180.10F

by Bahadir USA LLC

Bahadir USA Y180.10F is a Class I device made by Bahadir USA LLC, cleared under FDA 510(k) K131407 on 12 Aug 2014 and listed in FDA GUDID since 14 Aug 2017 (UDI-DI 00859982006889), active as of 22 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 22 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00859982006889 UDI-DI	Date14 Aug 2017Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated	NumberK131407	Date12 Aug 2014Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00859982006889
FDA 510(k) database 510(k) number K131407

Across registries

2 registries list this device

FDA 510(k) K131407 decided 12 Aug 2014 Active
FDA GUDID UDI-DI 00859982006889 listed 14 Aug 2017 Listed

Timeline

2 dated events

12 Aug 2014 Cleared FDA 510(k) K131407
14 Aug 2017 Listed FDA GUDID 00859982006889

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Bahadir USA
Generic name: Device sterilization/disinfection container, reusable
Model / reference: Y180.10F
Description: PERFORATED TRAY WITH FEET 484X252X110MM

Primary DI / UDI-DI: 00859982006889
510(k) Number: K131407
FDA product code: FSM
GMDN term: Device sterilization/disinfection container, reusable

Device class: Class I
Regulation number: 878.4800
GUDID distribution status: In Commercial Distribution

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Properties

Lot / batch number

Other properties (14, all answered No)