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Screening Tool (Terveyden riskitestit)

by Oiva Health Oy

Ref SCREENINGTOOL

Active European Union

CE MDR

Valid until

16 Jan 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS FIMKO OY

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number6429811363SCREENINGTOOL29 Basic UDI-DI 06429811363007UDI-DIDate28 Jan 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • FI26/0000002 Active

    Quality management system EU MDR

    Certifier
    SGS FIMKO OY 0598
    Issued
    16 Jan 2026
    Expires
    16 Jan 2031
    Valid from
    17 Jan 2026

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Screening Tool
Model / Reference
SCREENINGTOOL
Primary DI / UDI-DI
06429811363007
Basic UDI-DI
6429811363SCREENINGTOOL29
Direct Marketing DI
06429811363007
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class IIa
Special Device Type
Software
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000045801

Other devices from Oiva Health Oy

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Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No