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Zirconite

by B.J.M. Laboratories Ltd. 12 variants

Ref 400050PRO

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 linked in EUDAMED

A group certificate may exist

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 Number72901150510005099 Basic UDI-DI 07290115051018UDI-DIDate20 Jan 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Permanent Adhesive Cements
Model / Reference
400050PRO
Primary DI / UDI-DI
07290115051018
Basic UDI-DI
72901150510005099
EMDN Code
Q0101010299 Temporary and permanent dental restoration cements - other
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
IL-MF-000034121
Authorised representative
Obelis s.a. BE-AR-000000106

Related devices

Category: Dental composite resin

Other devices from B.J.M. Laboratories Ltd.

See all devices from B.J.M. Laboratories Ltd. →

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