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Brasseler USA 5013825U0

by Peter Brasseler Holdings, LLC

Brasseler USA 5013825U0 is a Class I device made by Peter Brasseler Holdings, LLC, listed in FDA GUDID since 1 Dec 2022 (UDI-DI 00887919580485), 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 Number00887919580485 UDI-DI Date1 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  • Withdrawn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
Root canal post, preformed
Model / reference
5013825U0
Primary DI / UDI-DI
00887919580485
FDA product code
ELR
GMDN term
Root canal post, preformed
Device class
Class I
Regulation number
872.3810
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Root canal post, preformed

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Other devices filed under Root canal post, preformed.

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Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)