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Kit per trattamento di REOFERESI DOPPIA FILTRAZIONE DA PAZIENTE

by Medica S.p.A.

Ref AF03631

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number803377232-AF03631-MK Basic UDI-DI 08033772328753UDI-DIDate2 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
AF03631
Primary DI / UDI-DI
08033772328753
Basic UDI-DI
803377232-AF03631-MK
EMDN Code
A020199, B030201
Device Class
Class IIb
Medical Purpose
DFPP / Rheopheresis (double filtration)

Manufacturer details

EUDAMED SRN
IT-PR-000029284

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Properties

  • Sterile