Skip to content

BasePlast Monomer 500ml

by Candulor AG

Ref 674271

BasePlast Monomer 500ml (674271) is a Class IIa device made by Candulor, AG, registered in EUDAMED on 9 Jul 2026 (Basic UDI-DI 763081342APROS004VJ), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number763081342APROS004VJ Basic UDI-DI 07630813461922UDI-DIDate9 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Autoplast, Baseplast, X PLEX
Model / reference
674271
Primary DI / UDI-DI
07630813461922
Basic UDI-DI
763081342APROS004VJ
EMDN code
Q010699 Materials for the preparation of custom-made dental devices - other
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000015795
Authorised representative
Candulor Dental GmbH DE-AR-000005472

Similar devices in this category

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

Other devices from Candulor, AG

See all devices from Candulor, AG →

Properties

Other properties (14, all answered No)