Skip to content

ENTstatistics

by Innoforce Anstalt Liechtenstein EUDAMED

Ref IMIS 6.3

EMDN V92,Z12129092,Z12149092

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number764029598IMISLQ Basic UDI-DIDate12 Sep 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • Z-24-137-S-IX Issued

    Quality management system EU MDR

    Notified body
    Notified body 0633
    Issued
    25 Aug 2025
    Expires
    14 Aug 2030

Specification

EUDAMED · synced 23 Oct 2026

Device Name
INNOFORCE Medical Information System
Model / Reference
IMIS 6.3
Primary DI / UDI-DI
07640295980026
Basic UDI-DI
764029598IMISLQ
Direct Marketing DI
07640295980026
EMDN Code
V92,Z12129092,Z12149092
Device Class
Class IIa
Special Device Type
Software
Market of Registration
Liechtenstein

Manufacturer details

EUDAMED SRN
LI-MF-000002047

Other devices from Innoforce Anstalt

See all devices from Innoforce Anstalt →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 07640295980026|764029598IMISLQ 61 fields · synced 23 Oct 2026