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Oravizio

by Solita Oy

Ref 20211109T084408Z-3dd28da3244fe788c9453bce521b378db3c7c55c

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-20211109T084408Z-3dd2RW Basic UDI-DI D-20211109T084408Z-3dd2RWUDI-DIDate13 Dec 2021RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDD Withdrawn

Specification

EUDAMED

Model / Reference
20211109T084408Z-3dd28da3244fe788c9453bce521b378db3c7c55c
Primary DI / UDI-DI
D-20211109T084408Z-3dd2RW
Basic UDI-DI
B-20211109T084408Z-3dd2RW
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class I
Special Device Type
-1192
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000017828

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: 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