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KA BGB- enlivio WebApp

by room4 Softwareentwicklung GmbH

Ref KA BGB- enlivio WebApp

Active European Union

CE MDR

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/MDR Number912014377ENLIVIOBASEX2 Basic UDI-DI 09120143773072UDI-DIDate23 Mar 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Enlivio
Model / Reference
KA BGB- enlivio WebApp
Primary DI / UDI-DI
09120143773072
Basic UDI-DI
912014377ENLIVIOBASEX2
EMDN Code
Z12069092 Various physiotherapy and rehabilitation instruments - medical device software
Device Class
Class I
Special Device Type
Software
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
AT-MF-000004591

Other devices from room4 Softwareentwicklung GmbH

See all devices from room4 Softwareentwicklung GmbH →

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