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Orthomed E® Bone Fixation Screws

by Orthomed E

Ref 6222015813053Model Osteosynthesis Screw-Plate Systems

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 Number62220158SM000001VV Basic UDI-DI 62220158130538UDI-DIDate23 Jun 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  • Withdrawn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
Bone Fixation Screws
Model / Reference
Osteosynthesis Screw-Plate Systems, 6222015813053
Primary DI / UDI-DI
62220158130538
Basic UDI-DI
62220158SM000001VV
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