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Ceramco® 3 Paste Opaque Shade Series C3-101

by Dentsply International

Ref 303010Model Paste Opaque Shade Series C3-101

Ceramco® 3 Paste Opaque Shade Series C3-101 (303010) is a device classified as Class IIa in the EU and Class II in the US made by Dentsply International, registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-D0013030100) and listed in FDA GUDID since 21 Sep 2016 (UDI-DI D0013030100), 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-D0013030100 Basic UDI-DI D0013030100UDI-DIDate5 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD0013030100 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-D0013030100 registered 5 Nov 2026 Active
  • FDA GUDID UDI-DI D0013030100 listed 21 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID D0013030100
  2. Registered EUDAMED B-D0013030100

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  • Withdrawn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 Shade Series Paste Opaque C3-101 2ml Syringe EUDAMED
Ceramco® 3 GUDID
Generic name
Dental appliance fabrication material, ceramic
Model / Ref / Catalog
Paste Opaque Shade Series C3-101, 303010
Primary DI / UDI-DI
D0013030100 EUDAMED
D0013030101 GUDID
Basic UDI-DI
B-D0013030100
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
Total Volume — 2 Milliliter

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
D0013030100
GUDID
D0013030101
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
Yes
GUDID
No

The registries describe this device under different primary UDI-DIs (EUDAMED lists D0013030100; FDA GUDID lists D0013030101), 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 PROSTHETIC DENTISTRY DEVICES - OTHER.

Other devices from Dentsply International

See all devices from Dentsply International →

Properties

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