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Aliamare

by Ibsa Farmaceutici Italia SRL 5 variants

Ref 8033638950029Model 73IS02

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 Number803363895RE0018Q Basic UDI-DI 08033638950029UDI-DIDate17 Apr 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  • Withdrawn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

Device Name
Rhinological and otological solution sea water and HA 0,2%
Model / Reference
73IS02, 8033638950029
Primary DI / UDI-DI
08033638950029
Basic UDI-DI
803363895RE0018Q
Direct Marketing DI
08033638950029
EMDN Code
Q0399 ENT devices - other
Device Class
Class IIa
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
IT-MF-000008111

Other devices from IBSA Farmaceutici Italia Srl

See all devices from IBSA Farmaceutici Italia Srl →

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