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Hahnenkratt 44602

by E. Hahnenkratt GmbH

Hahnenkratt 44602 is a Class I device made by E. Hahnenkratt GmbH, listed in FDA GUDID since 9 Sep 2024 (UDI-DI E206446021), 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 NumberE206446021 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  • Withdrawn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
Root canal post, preformed
Model / reference
44602
Primary DI / UDI-DI
E206446021
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

Similar devices in this category

Other devices filed under Root canal post, preformed.

Other devices from E. Hahnenkratt GmbH

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Properties

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