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MEDENTiKA H 30

by MEDENTiKA GmbH

Ref H 30Model Implant pick-up

MEDENTiKA H 30 is a Class I device made by MEDENTiKA GmbH, registered in EUDAMED on 29 Jul 2026 (Basic UDI-DI 42515748ABF0034N) and listed in FDA GUDID since 8 Apr 2020 (UDI-DI 04251574817037), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42515748ABF0034N Basic UDI-DI 04251574817037UDI-DIDate29 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04251574817037 UDI-DI Date8 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42515748ABF0034N registered 29 Jul 2026 Active
  • FDA GUDID UDI-DI 04251574817037 listed 8 Apr 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04251574817037
  2. Registered EUDAMED 42515748ABF0034N

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  • Withdrawn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

Trade name
MEDENTiKA
Generic name
Dental implant suprastructure, temporary, preformed, reusable
Model / Ref / Catalog
H 30, Implant pick-up
Primary DI / UDI-DI
04251574817037 EUDAMED
EMKAH309 GUDID
Basic UDI-DI
42515748ABF0034N
FDA product code
NDP
EMDN code
Q010599 Dental instruments, single-use - other
GMDN term
Dental implant suprastructure, temporary, preformed, reusable
Device class
Class I
Regulation number
872.3980
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Conditional

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
04251574817037
GUDID
EMKAH309
ImplantableEUDAMED
No
GUDID
Yes

The registries describe this device under different primary UDI-DIs (EUDAMED lists 04251574817037; FDA GUDID lists EMKAH309), so their flags are not compared.

Related devices

Category: Dental implant suprastructure, temporary, preformed, reusable

Similar devices in this category

Other devices filed under DENTAL INSTRUMENTS, SINGLE-USE - OTHER.

Other devices from MEDENTiKA GmbH

See all devices from MEDENTiKA GmbH →

Properties

  • Sterilise before use
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)