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CARPEDIEM Cardio Renal Pediatric Dealysis Emergency Machine

by Bellco s.r.l. 2 variants

Ref IB7010250

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 Number0763000B00000116K Basic UDI-DI 08032979795184UDI-DIDate25 May 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
Carpediem
Model / Reference
IB7010250
Primary DI / UDI-DI
08032979795184
Basic UDI-DI
0763000B00000116K
Direct Marketing DI
08032979795184
EMDN Code
Z12090301 Haemofiltration equipment
Device Class
Class IIb

Manufacturer details

EUDAMED SRN
IT-MF-000022065

Other devices from Bellco s.r.l.

See all devices from Bellco s.r.l. →

Properties

  • Reusable
  • Administering Medicine
  • Measuring Function

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Incorporates Medicinal Product: No