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Contivue®

by F. Hoffmann-La Roche Ltd. EUDAMED

Active European Union

Ref 4000158

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number08100425932120_III_0001QG Basic UDI-DIDate27 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Specification

EUDAMED

Device Name
Contivue® Implant with Ita (Insertion Tool Assembly)
Model / Reference
4000158
Primary DI / UDI-DI
00810042590106
Basic UDI-DI
08100425932120_III_0001QG
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000041950
Authorised representative
MedEnvoy Global BV NL-AR-000024028

Other devices from F. Hoffmann-La Roche Ltd.

Properties

  • Sterile
  • Implantable
  • Administering Medicine

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No