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Covision

by Covision Medical Technologies Ltd. 123 variants

Ref 95.0902Model PARAGON INSTRUMENT CASE2

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05051659188484 Basic UDI-DI 05051659188484UDI-DIDate5 Jun 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  • Withdrawn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

Device Name
Paragon Instrument CASE2
Model / Reference
PARAGON INSTRUMENT CASE2, 95.0902
Primary DI / UDI-DI
05051659188484
Basic UDI-DI
B-05051659188484
EMDN Code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device Class
Class I
Market of Registration
Austria

Manufacturer details

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

Other devices from Covision Medical Technologies Ltd.

See all devices from Covision Medical Technologies Ltd. →

Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: 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