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Orthomed E® Bone Fixation Plates

by Orthomed E 46 variants

Ref 6222049655797Model Anatomical Bone Plates

Active European Union

CE MDR

Valid until

7 Dec 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

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 Number62220158PM300043VT Basic UDI-DI 62220496557974UDI-DIDate2 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Bone Fixation Plates
Model / Reference
Anatomical Bone Plates, 6222049655797
Primary DI / UDI-DI
62220496557974
Basic UDI-DI
62220158PM300043VT
Direct Marketing DI
62220496557974
EMDN Code
P09120503 Osteosynthesis screw-plate systems
Device Class
Class IIb
EU market of registration
Cyprus

Manufacturer details

EUDAMED SRN
EG-MF-000011052
Authorised representative
Osseous Ltd CY-AR-000044017

Other devices from Orthomed E

See all devices from Orthomed E →

Properties

  • Implantable
  • Reprocessed
  • Sutures

Other properties (11)

  • Sterile: No
  • Reusable: No
  • Contains Latex: 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