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Imphora

by Standard Instruments GmbH Germany EUDAMED

Ref SI-ZNIS-M

EMDN G030799

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426018106VRMPA8 Basic UDI-DIDate7 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
ViMeDat Reflux- und Motilitätsanalyse-Plattform
Model / Reference
SI-ZNIS-M
Primary DI / UDI-DI
04260181060088
Basic UDI-DI
426018106VRMPA8
EMDN Code
G030799 Gastrointestinal endoscopy, diagnostic devices - other
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000013833

Other devices from Standard Instruments GmbH

See all devices from Standard Instruments GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • Measuring Function
Other properties (12)
  • 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
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 4f30d8f1-88a4-47c2-ba1c-e8a7e40910be 61 fields · synced 22 Oct 2026