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UpHill Route

by Uphill S.A.

Ref UpHill Route

Active European Union

CE MDR

Valid until

23 Jan 2030

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier Intertek Medical Notified Body AB

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number56001398890DSSW9 Basic UDI-DI 05600139889009UDI-DIDate10 Mar 2026RegisteredStatusActive

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • 28620203207 Active Removed from EUDAMED

    Quality management system EU MDR

    Issued
    24 Jan 2025
    Expires
    23 Jan 2030
  • 28620203207 Active Supplemented

    Quality management system EU MDR

    Issued
    24 Jan 2025
    Expires
    23 Jan 2030
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
UpHill Route
Primary DI / UDI-DI
05600139889009
Basic UDI-DI
56001398890DSSW9
Direct Marketing DI
05600139889009
EMDN Code
V92 Medical device software - not included in other classes
Device Class
Class IIa
Special Device Type
Software
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000021496

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