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Orthomed E® Bone Fixation Plates

by Orthomed E 46 variants

Ref 6222049650518Model Straight 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number62220158PM300008VR Basic UDI-DI 62220496505180UDI-DIDate1 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  • Withdrawn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
Straight Bone Plates, 6222049650518
Primary DI / UDI-DI
62220496505180
Basic UDI-DI
62220158PM300008VR
Direct Marketing DI
62220496505180
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