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Hu-Friedy

by Hu-Friedy Manufacturing Co., LLC 1,000+ variants

Part of a family of 113 devices: see the family page

Ref TNANTKITModel Kit

Hu-Friedy (TNANTKIT) is a Class I device made by Hu-Friedy Manufacturing Co., LLC, registered in EUDAMED on 15 Aug 2025 (Basic UDI-DI 0889950Kit1FZ) and listed in FDA GUDID since 12 Nov 2020 (UDI-DI 10889950033606), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0889950Kit1FZ Basic UDI-DI 10889950033606UDI-DIDate15 Aug 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10889950033606 UDI-DI Date12 Nov 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0889950Kit1FZ registered 15 Aug 2025 Active
  • FDA GUDID UDI-DI 10889950033606 listed 12 Nov 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10889950033606
  2. Registered EUDAMED 0889950Kit1FZ

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
Kit, TNANTKIT
Primary DI / UDI-DI
10889950033606
Basic UDI-DI
0889950Kit1FZ
FDA product code
EIY
EMDN code
Q0199 Odontology devices - other
GMDN term
Dental/maxillofacial surgical procedure kit, non-medicated, reusable
Device class
Class I
Regulation number
872.4565
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
US-MF-000017104
Authorised representative
Hu-Friedy Europe LLC & Co. KG DE-AR-000005530

Similar devices in this category

Other devices filed under ODONTOLOGY DEVICES - OTHER.

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Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (22, all answered No)