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nasal aspirator

by Cotronic Technology Ltd EUDAMED

Active European Union

Ref ASPI 2Model ASPI,ASPI2,ASPI3,ASPI-V

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69333457nasalaspiratorYP Basic UDI-DIDate2 Apr 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
nasal aspirator
Model / Reference
ASPI,ASPI2,ASPI3,ASPI-V, ASPI 2
Primary DI / UDI-DI
06933345720026
Basic UDI-DI
69333457nasalaspiratorYP
Direct Marketing DI
06933345720026
EMDN Code
R05010399 Mucosity aspirators - other
Device Class
Class I
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
CN-MF-000023700
Authorised representative
Share info GmbH DE-AR-000005132

Other devices from Cotronic Technology Limited

See all devices from Cotronic Technology Limited →

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