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OMNIset ECCO2R

by B. Braun Avitum AG

Ref 7211607

OMNIset ECCO2R (7211607) is a Class IIb device made by B.Braun Avitum AG, registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI 403923900000247938), 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 Number403923900000247938 Basic UDI-DI 04046955869114UDI-DIDate3 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
OMNIset ECCO2R with ECCO2R
Model / reference
7211607
Primary DI / UDI-DI
04046955869114
Basic UDI-DI
403923900000247938
EMDN code
C030199 Extracorporeal and assisted circulation devices - other
Device class
Class IIb
System or procedure pack
Procedure pack
EU registration type
System or procedure pack
Medical purpose
Kit for continuous acute blood purification treatments for patients with acute renal failure and/or intoxication

Manufacturer details

EUDAMED SRN
DE-PR-000005128

Similar devices in this category

Other devices filed under EXTRACORPOREAL AND ASSISTED CIRCULATION DEVICES - OTHER.

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Properties

Other properties (2, all answered No)