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Apteczka ABC NaCI 3% hipertoniczny roztwór do inhalacji

by Laboratoire Unither

Ref 5 902666 654854Model Sterile hypertonic solution of sodium chloride 3% in vials for inhalation

Active European Union

CE MDD

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/MDD NumberB-59026666548547S Basic UDI-DI D-59026666548547SUDI-DIDate21 Oct 2024RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
Sterile hypertonic solution of sodium chloride 3% in vials for inhalation, 5 902666 654854
Primary DI / UDI-DI
D-59026666548547S
Basic UDI-DI
B-59026666548547S
EMDN Code
R0699 Nebulisation and humidification systems - other
Device Class
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
FR-MF-000004062

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Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No