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Reflecto Tibial Augment L.m/R.l Size 3 X 15 Mm

by Covision Medical Technologies Ltd.

Ref 01.9903Model REFLECTO TIBIAL AUGMENT L.M/R.L SIZE 3 X 15 MM

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05051659178799 Basic UDI-DI 05051659178799UDI-DIDate2 May 2023RegisteredStatusActive

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  • Withdrawn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
REFLECTO TIBIAL AUGMENT L.M/R.L SIZE 3 X 15 MM, 01.9903
Primary DI / UDI-DI
05051659178799
Basic UDI-DI
B-05051659178799
EMDN Code
P09098001 Knee prostheses augments
Device Class
Class III
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
GB-MF-000025081
Authorised representative
Covision Medical Technologies (Ireland) Limited IE-AR-000031129

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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