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Brasseler USA 5025491U0

by Peter Brasseler Holdings, LLC

Brasseler USA 5025491U0 is a Class I device made by Peter Brasseler Holdings, LLC, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 00887919760900), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00887919760900 UDI-DI Date8 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Brasseler USA
Generic name
Periotome, reusable
Model / reference
5025491U0
Primary DI / UDI-DI
00887919760900
FDA product code
EMJ
GMDN term
Periotome, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Periotome, reusable

Other devices from Peter Brasseler Holdings, LLC

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)