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S dispensing line

by AEA srl

Ref SDL-01-FIL

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 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

    Certifier
    KIWA CERMET ITALIA S.P.A. 0476
    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  • Withdrawn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

Model / Reference
SDL-01-FIL
Primary DI / UDI-DI
05060304051035
Basic UDI-DI
506030405SDLAU
EMDN Code
A0399 Tubular devices - other
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IT-MF-000027519

Other devices from Aea SRL

See all devices from Aea SRL →

Properties

  • Sterile

Other properties (12)

  • 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