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Depression Health Risk Questionnaire

by Movendos Oy 3 variants

Ref MQ-DEPR-181416Model 181416

Withdrawn Withdrawn in European Union.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Was authorized under CE MDD, withdrawn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Withdrawn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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-MQ-DEPR-181416HD Basic UDI-DI D-MQ-DEPR-181416HDUDI-DIDate8 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  • Withdrawn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European Union — CE/MDD Withdrawn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

Device Name
Depression Health Risk Questionnaire
Model / Reference
181416, MQ-DEPR-181416
Primary DI / UDI-DI
D-MQ-DEPR-181416HD
Basic UDI-DI
B-MQ-DEPR-181416HD
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-000006465

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