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Ventway Sparrow Rechargeable Battery

by Inovytec Medical Solutions Ltd.

Ref VWSP-420

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 Number7290017096VentwayRBZC Basic UDI-DI 07290017096360UDI-DIDate11 Jun 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  • Withdrawn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
Ventway Sparrow Rechargeable Battery
Model / Reference
VWSP-420
Primary DI / UDI-DI
07290017096360
Basic UDI-DI
7290017096VentwayRBZC
EMDN Code
Z1203019099 Various instruments for anaesthesia and pulmonary ventilation support – other
Device Class
Class I
EU market of registration
Denmark

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