Brasseler USA 5003753M0

by Peter Brasseler Holdings, LLC

Brasseler USA 5003753M0 is a Class I device made by Peter Brasseler Holdings, LLC, listed in FDA GUDID since 1 Dec 2022 (UDI-DI 00887919437604), 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	Number00887919437604 UDI-DI	Date1 Dec 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00887919437604

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Brasseler USA
Generic name: Surgical saw blade, oscillating, single-use
Model / reference: 5003753M0

Primary DI / UDI-DI: 00887919437604
FDA product code: GFA
GMDN term: Surgical saw blade, oscillating, single-use

Device class: Class I
Regulation number: 878.4820
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Supplied sterile
Sterilise before use
Single use
Prescription use
Premarket exempt
Lot / batch number
Expiration date

Other properties (8, all answered No)