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Ceramco® 3 Powder Opaque D3

by Dentsply International

Ref 301022Model Powder Opaque D3

Ceramco® 3 Powder Opaque D3 (301022) is a device classified as Class IIa in the EU and Class II in the US made by Dentsply International, registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI B-D0013010220) and listed in FDA GUDID since 21 Sep 2016 (UDI-DI D0013010220), 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-D0013010220 Basic UDI-DI D0013010220UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD0013010220 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-D0013010220 registered 2 Nov 2026 Active
  • FDA GUDID UDI-DI D0013010220 listed 21 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID D0013010220
  2. Registered EUDAMED B-D0013010220

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  • Withdrawn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
C3 POWDER OPAQUE D3 1oz EUDAMED
Ceramco® 3 GUDID
Generic name
Dental appliance fabrication material, ceramic
Model / Ref / Catalog
Powder Opaque D3, 301022
Primary DI / UDI-DI
D0013010220 EUDAMED
D0013010221 GUDID
Basic UDI-DI
B-D0013010220
FDA product code
EIH
EMDN code
Q010299 Prosthetic dentistry devices - other
GMDN term
Dental appliance fabrication material, ceramic
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
872.6660
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Weight — 28.4 Gram

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
D0013010220
GUDID
D0013010221
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

The registries describe this device under different primary UDI-DIs (EUDAMED lists D0013010220; FDA GUDID lists D0013010221), so their flags are not compared. 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: Dental appliance fabrication material, ceramic

Similar devices in this category

Other devices filed under DEVICES FOR PROSTHETIC DENTISTRY.

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Properties

  • Implantable YesEUDAMEDNoGUDID
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)