Gpc BHF1248

by Gpc Medical, Ltd.

Gpc BHF1248 is a Class I device made by Gpc Medical, Ltd., listed in FDA GUDID since 23 May 2024 (UDI-DI 08904400200676), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number08904400200676 UDI-DI	Date23 May 2024Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 08904400200676

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Gpc
Generic name: General external orthopaedic fixation system implantation kit, reusable
Model / reference: BHF1248

Primary DI / UDI-DI: 08904400200676
FDA product code: LXH
GMDN term: General external orthopaedic fixation system implantation kit, reusable

Device class: Class I
Regulation number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Other devices filed under General external orthopaedic fixation system implantation kit, reusable.

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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number
Manufacturing date

Other properties (10, all answered No)