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C-Plast 672722

by Candulor AG

Ref 672722

C-Plast 672722 is a dental base plate (EU MDR Class I; FDA Class I; FDA product code EBH, Material, Impression Tray, Resin) made by Candulor AG, registered in EUDAMED on 9 Oct 2026 (Basic UDI-DI 763081341XTRAY0018Z) and listed in FDA GUDID since 14 Nov 2022 (UDI-DI 07630813440033), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number763081341XTRAY0018Z Basic UDI-DI 07630813440033UDI-DIDate9 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07630813440033 UDI-DI Date14 Nov 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 763081341XTRAY0018Z registered 9 Oct 2026 Active
  • FDA GUDID UDI-DI 07630813440033 listed 14 Nov 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07630813440033
  2. Registered EUDAMED 763081341XTRAY0018Z

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  • Withdrawn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
C-Plast Polymer 500g F34 EUDAMED
C-Plast GUDID
Generic name
Dental base plate
Model / Ref / Catalog
672722
Primary DI / UDI-DI
07630813440033
Basic UDI-DI
763081341XTRAY0018Z
FDA product code
EBH
EMDN code
Q010699 Materials for the preparation of custom-made dental devices - other
GMDN term
Dental base plate
Device class
Class I
Regulation number
872.3670
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER.

Other devices from Candulor AG

See all devices from Candulor AG →

Properties

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