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GHG Praxisdienst Medizinische Scores

by ifap Service-Institut für Ärzte und Apotheker GmbH 2 variants

Ref ab R4.1

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-1311682TFMEDSCORES4.161 Basic UDI-DI 1311682TFMEDSCORES4.161UDI-DIDate12 May 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  • Withdrawn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
THERAFOX PRO GHG Praxisdienst Medizinische Scores
Model / Reference
ab R4.1
Primary DI / UDI-DI
1311682TFMEDSCORES4.161
Basic UDI-DI
B-1311682TFMEDSCORES4.161
EMDN Code
Z12040292 General medicine therapeutic treatment instruments - medical device software
Device Class
Class I
Special Device Type
-1192
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006908

Other devices from ifap Service-Institut für Ärzte und Apotheker GmbH

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