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Hahnenkratt 10054

by E. Hahnenkratt GmbH

Hahnenkratt 10054 is a Class I device made by E. Hahnenkratt GmbH, listed in FDA GUDID since 9 Sep 2024 (UDI-DI E206100540), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberE206100540 UDI-DI Date9 Sep 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Hahnenkratt
Generic name
Dental matrix band, reusable
Model / reference
10054
Primary DI / UDI-DI
E206100540
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

Related devices

Category: Dental matrix band, reusable

Similar devices in this category

Other devices filed under Dental matrix band, reusable.

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Properties

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