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Maxi Z Implant

by OsteoCare Implant System Limited 6 variants

Ref IM-MAXZ550-130Model Implants

Active European Union

CE MDD

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/MDD NumberB-50609129505912 Basic UDI-DI 50609129505912UDI-DIDate8 Oct 2024RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
Implants, IM-MAXZ550-130
Primary DI / UDI-DI
50609129505912
Basic UDI-DI
B-50609129505912
EMDN Code
P01020101 Dental implants
Device Class
Class IIb
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000016843
Authorised representative
Advena Limited MT-AR-000000234

Other devices from OsteoCare Implant System Limited

See all devices from OsteoCare Implant System Limited →

Properties

  • Sterile
  • Implantable

Other properties (9)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No