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Preassembled device 025

by Bellco s.r.l.

Ref IB0580805Model Kit CVVH/CVVHD

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 Number0763000B000006376 Basic UDI-DI 38032979796229UDI-DIDate5 Aug 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  • Withdrawn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
Kit CVVH/CVVHD, IB0580805
Primary DI / UDI-DI
38032979796229
Basic UDI-DI
0763000B000006376
EMDN Code
Z12090285, Z12090385
Device Class
Class IIb
Medical Purpose
Procedure pack for hemofiltration (CVVH) and hemodialysis (CVVHD)

Manufacturer details

EUDAMED SRN
IT-PR-000022066

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Properties

Other properties (1)

  • Sterile: No