Surgical Direct SD914709156

by Surgical Direct, Inc.

Surgical Direct SD914709156 is a Class I device made by Surgical Direct, Inc., listed in FDA GUDID since 1 Dec 2022 (UDI-DI B382SD9147091560), 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	NumberB382SD9147091560 UDI-DI	Date1 Dec 2022Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Surgical Direct
Generic name: Periosteal elevator, reusable
Model / Ref / Catalog: SD914709156

Primary DI / UDI-DI: B382SD9147091560
FDA product code: GEG
GMDN term: Periosteal elevator, reusable

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

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Premarket exempt
Lot / batch number

Other properties (12, all answered No)