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Diapact CRRT

by B. Braun Avitum AG 23 variants

Ref 7211545

Diapact CRRT (7211545) is a Class IIa device made by B.Braun Avitum AG, registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 40392390000033552U), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number40392390000033552U Basic UDI-DI 04046955718405UDI-DIDate2 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Diapact CRRT - Lines for Blood treatment
Model / reference
7211545
Primary DI / UDI-DI
04046955718405
Basic UDI-DI
40392390000033552U
EMDN code
F020180 Arteriovenous dialysis lines for haemodialysis - haemofiltration -haemodiafiltration - accessories
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005127

Similar devices in this category

Other devices filed under ARTERIOVENOUS DIALYSIS LINES FOR HAEMODIALYSIS - HAEMOFILTRATION -HAEMODIAFILTRATION.

Other devices from B.Braun Avitum AG

See all devices from B.Braun Avitum AG →

Properties

  • Supplied sterile
Other properties (13, all answered No)