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Alvita Nazal Aspiratör (FR)

by İyon Sağlik Medi̇kal Kozmeti̇k İthalat İhracat Ve Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇

Ref NASP01

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number869924177NASPUQ Basic UDI-DI 86849351208228UDI-DIDate20 Jan 2025RegisteredStatusActive

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  • Withdrawn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
Nasal Aspirator
Model / Reference
NASP01
Primary DI / UDI-DI
86849351208228
Basic UDI-DI
869924177NASPUQ
EMDN Code
R05010399 Mucosity aspirators - other
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
TR-MF-000027085

Other devices from İyon Sağlik Medi̇kal Kozmeti̇k İthalat İhracat Ve Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇

See all devices from İyon Sağlik Medi̇kal Kozmeti̇k İthalat İhracat Ve Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ →

Properties

  • Incorporates Medicinal Product

Other properties (12)

  • 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