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Gonioscopy Lens

by Volk Optical Inc. 5 variants

Part of a family of 33 devices: see the family page

Ref VEG3

Gonioscopy Lens (VEG3) is a medical device (EU MDR Class I; EMDN category ophtalmology assessments and diagnosis instruments – other) made by Volk Optical Inc., registered in EUDAMED on 5 Feb 2026 (Basic UDI-DI 81160801GONIOGU), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number81160801GONIOGU Basic UDI-DI 00811608019222UDI-DIDate5 Feb 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Gonioscopy Lens
Model / reference
VEG3
Primary DI / UDI-DI
00811608019222
Basic UDI-DI
81160801GONIOGU
Direct marketing DI
00811608019222
EMDN code
Z12120199 Ophtalmology assessments and diagnosis instruments – other
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000017843
Authorised representative
Rudolf Riester GmbH DE-AR-000015844

Similar devices in this category

Other devices filed under OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER.

Other devices from Volk Optical Inc.

See all devices from Volk Optical Inc. →

Properties

Other properties (14, all answered No)