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Patient Circuit

by Inovytec Medical Solutions Ltd. 5 variants

Ref VWSP-1370Model Ventway Sparrow Patient Circuit

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7290017096VentwayPCZ8 Basic UDI-DI 17290017096886UDI-DIDate11 Feb 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
Ventway Sparrow Patient Circuit, VWSP-1370
Primary DI / UDI-DI
17290017096886
Basic UDI-DI
7290017096VentwayPCZ8
EMDN Code
R020199 Breathing circuits and kits - other
Device Class
Class IIa
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
IL-MF-000034055
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Inovytec Medical Solutions Ltd.

See all devices from Inovytec Medical Solutions Ltd. →

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