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Ah 26 60620002

by Dentsply De Trey GmbH

Ref 60620002

Ah 26 60620002 is a device classified as Class IIa in the EU and Class II in the US made by Dentsply De Trey GmbH, registered in EUDAMED on 22 Oct 2026 (Basic UDI-DI B-D010606200021) and listed in FDA GUDID since 20 Sep 2016 (UDI-DI D010606200021), active as of 7 Nov 2026.

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

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-D010606200021 Basic UDI-DI D010606200021UDI-DIDate22 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD010606200021 UDI-DI Date20 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-D010606200021 registered 22 Oct 2026 Active
  • FDA GUDID UDI-DI D010606200021 listed 20 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID D010606200021
  2. Registered EUDAMED B-D010606200021

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
AH 26 Resin Refill EUDAMED
Ah 26 GUDID
Generic name
Endodontic filling/sealing material
Model / Ref / Catalog
60620002
Primary DI / UDI-DI
D010606200021
Basic UDI-DI
B-D010606200021
FDA product code
KIF
EMDN code
Q01010202 Root canal filling dental cements
GMDN term
Endodontic filling/sealing material
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.3820
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Weight — 10 Gram

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Endodontic filling/sealing material

Similar devices in this category

Other devices filed under ROOT CANAL FILLING DENTAL CEMENTS.

Other devices from Dentsply De Trey GmbH

See all devices from Dentsply De Trey GmbH →

Properties

  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (20, all answered No)