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Patient Lift Sling

by Yingkou Henyi Flow Control Inc China EUDAMED

Ref AuraModel Aura / Luma / Nova / Viva EMDN V0805038002

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697463134PLiftSlingR3 Basic UDI-DIDate21 May 2025RegisteredStatusActive

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  • Withdrawn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
Patient Lift Sling
Model / Reference
Aura / Luma / Nova / Viva, Aura
Primary DI / UDI-DI
06974631340009
Basic UDI-DI
697463134PLiftSlingR3
EMDN Code
V0805038002 Non-rigid supports for lifts (harnesses)
Device Class
Class I
Market of Registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000009000
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Yingkou Henyi Flow Control Inc

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 741d3271-612f-45b2-a710-4ac1ca525187 61 fields · synced 22 Oct 2026