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Walser® matrices 0acd

by Dr. Walser Dental GmbH

Walser® matrices 0acd is a Class I device made by Dr. Walser Dental GmbH, listed in FDA GUDID since 1 Dec 2025 (UDI-DI 04262363910792), 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 Number04262363910792 UDI-DI Date1 Dec 2025ListedStatusListed 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  • Withdrawn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
Walser® matrices
Generic name
Dental matrix band, reusable
Model / reference
0acd
Primary DI / UDI-DI
04262363910792
FDA product code
DZN
GMDN term
Dental matrix band, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code DZN (Instruments, Dental Hand).

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Properties

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