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Diapact CRRT

by B. Braun Avitum Italy S.p.A

Ref 7211522

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40392390000024802R Basic UDI-DI 04046955724406UDI-DIDate15 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  • Withdrawn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

Device Name
Diapact CRRT Kit (PP)
Model / Reference
7211522
Primary DI / UDI-DI
04046955724406
Basic UDI-DI
40392390000024802R
EMDN Code
F0303 Haemodialysis kits
Device Class
Class IIb
Medical Purpose
Hemofiltration/hemodialysis kit with Dializer and accessories

Manufacturer details

EUDAMED SRN
IT-PR-000010737

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Properties

Other properties (1)

  • Sterile: No