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Ca-800

by Visia imaging SRL

Ref 1248005

Ca-800 (1248005) is a Class IIa device made by Visia Imaging SRL, registered in EUDAMED on 8 Jul 2026 (Basic UDI-DI B-08034028770197), active as of 25 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08034028770197 Basic UDI-DI 08034028770197UDI-DIDate8 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
1248005
Primary DI / UDI-DI
08034028770197
Basic UDI-DI
B-08034028770197
EMDN code
Z12120123 Computerised corneal topographs
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000015628

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Properties

Other properties (12, all answered No)