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Blu 5029474U0

by Peter Brasseler Holdings, LLC

Blu 5029474U0 is a Class II device made by Peter Brasseler Holdings, LLC, listed in FDA GUDID since 15 Apr 2022 (UDI-DI 00887919929161), 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 Number00887919929161 UDI-DI Date15 Apr 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  • Withdrawn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
Blu
Generic name
Dental diode laser system
Model / reference
5029474U0
Primary DI / UDI-DI
00887919929161
FDA product code
GEX
GMDN term
Dental diode laser system
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

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Category: Dental diode laser system

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Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)