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Helpmedi NebuCare.Family zestaw nebulizator+sól fizjologiczna

by Actia Sp. z o.o.

Ref 5905490810175

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5905490810HNCF73 Basic UDI-DI 05905490810175UDI-DIDate30 Jan 2026RegisteredStatusActive

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  • Withdrawn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
5905490810175
Primary DI / UDI-DI
05905490810175
Basic UDI-DI
5905490810HNCF73
EMDN Code
R0699 Nebulisation and humidification systems - other
Device Class
Class IIa
Medical Purpose
Zestaw do nebulizacji i pielęgnacji dróg oddechowych. Zestaw zawiera wyroby medyczne oznakowane znakiem CE tj.: 1) Wyrób medyczny, KATAREK roztwór soli fizjologiczny NaCI 0,9% 20x5ml, którego producentem jest firma Laboratoire Unither, 2) Wyrób medyczny, Nebulizator siateczkowy NE-M01L/ Mesh Nebulizer NE-M01L producenta Contec Medical Systems Co., Ltd.

Manufacturer details

EUDAMED SRN
PL-PR-000037709

Other devices from ACTIA Sp. z o.o.

Properties

Other properties (1)

  • Sterile: No