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Dosing device 50ml

by AEA srl

Ref ASN-50-P

Expiring European Union

CE MDR

Valid until

9 Aug 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier KIWA CERMET ITALIA S.P.A.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberMDR 00004-A Date12 Oct 2026IssuedStatusExpiring expires 9 Aug 2027

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 00004-A Expiring Expires in 281 days

    Quality management system EU MDR

    Issued
    12 Oct 2026
    Expires
    9 Aug 2027

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
Dosing Device
Model / Reference
ASN-50-P
Primary DI / UDI-DI
05060304051271
Basic UDI-DI
506030405ASN9K
EMDN Code
A020102020101 Infusion and irrigation syringes, luer lock cone, 3-piece with needle, single-use
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000027519

Other devices from Aea SRL

See all devices from Aea SRL →

Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No