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Vantage Plus Himag

by Keeler Ltd

Ref 1202-P-7192

Vantage Plus Himag (1202-P-7192) is a medical device (EU MDR Class I) made by Keeler Ltd, registered in EUDAMED on 26 Aug 2026 (Basic UDI-DI 50552727LENSN9), 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 Number50552727LENSN9 Basic UDI-DI 05055272701174UDI-DIDate26 Aug 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  • Withdrawn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
Lenses
Model / reference
1202-P-7192
Primary DI / UDI-DI
05055272701174
Basic UDI-DI
50552727LENSN9
EMDN code
Z12120180 Ophtalmology assessments and diagnosis instruments - hardware accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GB-MF-000009031
Authorised representative
Keeler Europe Distribution, S.L. ES-AR-000001559

Similar devices in this category

Other devices filed under OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS - HARDWARE ACCESSORIES.

Other devices from Keeler Ltd

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Properties

Other properties (14, all answered No)