Skip to content

Scanbody

by Biodenta Swiss AG 5 variants

Ref CAD-SB3ILPA3456Model CAD-SBBBLB0

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0764016973CADSBVV Basic UDI-DI 07640169735790UDI-DIDate21 Mar 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Cad-SBBBLB0
Model / Reference
CAD-SBBBLB0, CAD-SB3ILPA3456
Primary DI / UDI-DI
07640169735790
Basic UDI-DI
0764016973CADSBVV
EMDN Code
Q010207 Dental impression devices for prosthetic dentistry
Device Class
Class I
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
CH-MF-000034374
Authorised representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Related devices

Category: Dental implant suprastructure, temporary, preformed, single-use

Other devices from Biodenta Swiss AG

See all devices from Biodenta Swiss AG →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No