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Raskauden Aikaisen Diabeteksen Seulonta Rv 22-24

by Oy Apotti Ab

Ref OLL0001120 RASKAUDEN AIKAISEN DIABETEKSEN SEULONTA RV 22-24

Withdrawn Withdrawn in European Union.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Was authorized under CE MDD, withdrawn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Withdrawn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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-OLL0001120MW Basic UDI-DI D-OLL0001120MWUDI-DIDate21 Feb 2024RegisteredStatusWithdrawn 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  • Withdrawn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European Union — CE/MDD Withdrawn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

Device Name
Raskauden Aikaisen Diabeteksen Seulonta Rv 22-24
Model / Reference
OLL0001120 RASKAUDEN AIKAISEN DIABETEKSEN SEULONTA RV 22-24
Primary DI / UDI-DI
D-OLL0001120MW
Basic UDI-DI
B-OLL0001120MW
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class I
Special Device Type
-1192

Manufacturer details

EUDAMED SRN
FI-MF-000007544

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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