Identity™ SBHTST12

by Zimmer, Inc.

Identity™ SBHTST12 is a Class I device made by Zimmer, Inc., listed in FDA GUDID since 22 Sep 2022 (UDI-DI 00889024627888), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00889024627888 UDI-DI	Date22 Sep 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00889024627888

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Identity™
Generic name: Reverse shoulder cup prosthesis trial, reusable
Model / Ref / Catalog: SBHTST12

Primary DI / UDI-DI: 00889024627888
FDA product code: HWT
GMDN term: Reverse shoulder cup prosthesis trial, reusable

Device class: Class I
Regulation number: 888.4800
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)