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GlucoTab R8.1

by decide Clinical Software GmbH Austria EUDAMED

Ref GlucoTab R8.1 EMDN Z12040292

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number918000023GT20-11AQG Basic UDI-DIDate21 Oct 2021RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
GlucoTab
Model / Reference
GlucoTab R8.1
Primary DI / UDI-DI
09180000230032
Basic UDI-DI
918000023GT20-11AQG
Direct Marketing DI
09180000230032
EMDN Code
Z12040292 General medicine therapeutic treatment instruments - medical device software
Device Class
Class IIa
Special Device Type
Software
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
AT-MF-000001001

Other devices from decide Clinical Software GmbH

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 c4921655-82a1-4ed7-921f-181fbcf6c560 61 fields · synced 22 Oct 2026