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Depression Health Risk Questionnaire

by Oiva Health Oy 4 variants

Ref MQ-DEPR-786568Model 786568

Active European Union

CE MDD

Valid until

Not listed

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

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/MDD NumberB-MQ-DEPR-786568-XE Basic UDI-DI D-MQ-DEPR-786568-XEUDI-DIDate2 Jan 2025RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
Depression Health Risk Questionnaire
Model / Reference
786568, MQ-DEPR-786568
Primary DI / UDI-DI
D-MQ-DEPR-786568-XE
Basic UDI-DI
B-MQ-DEPR-786568-XE
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-000045801

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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