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Prescriptor

by Digitalis Rx BV EUDAMED

Active European Union

Ref Prescriptor, 2Model Prescriptor 3

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number87208924574Prescriptor6J Basic UDI-DIDate26 Nov 2025RegisteredStatusActive
European UnionCE/MDR Number87208924574Prescriptor6J Basic UDI-DIDate26 Nov 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Model / Reference
Prescriptor 3, Prescriptor, 2
Primary DI / UDI-DI
08720892457400, D-10023674Prescriptor5F
Basic UDI-DI
87208924574Prescriptor6J, B-10023674Prescriptor5F
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class IIa
Class I
Special Device Type
Software
-1192
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000005888

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