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Biopax Neussnuiter / Mouche bébé

by Asia Connection Co., Ltd.

Ref BIO SNUModel ME4437/ME4438/ME4439

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 Number471987228ME443XE9 Basic UDI-DI 04719872280651UDI-DIDate20 Jan 2026RegisteredStatusActive

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  • Withdrawn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
Manual Nasal Aspirator
Model / Reference
ME4437/ME4438/ME4439, BIO SNU
Primary DI / UDI-DI
04719872280651
Basic UDI-DI
471987228ME443XE9
EMDN Code
R05010301 Single-chamber mucous membrane aspirators
Device Class
Class I
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
TW-MF-000006739
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Asia Connection Co., Ltd.

See all devices from Asia Connection Co., Ltd. →

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