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Congelatori per La Conservazione Di Sangue, Emoderivati E Plasma

by KW Apparecchi Scientifici Srl 86 variants

Ref KBPF HGD 600Model KBPF HGD 600, KBPF HGD 400

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 Number805750615CG005ZU Basic UDI-DI 08057506152032UDI-DIDate21 May 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  • Withdrawn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
KBPF HGD 600, KBPF HGD 400
Primary DI / UDI-DI
08057506152032
Basic UDI-DI
805750615CG005ZU
Direct Marketing DI
08057506152032
EMDN Code
Z121702 Blood and blood components freezers
Device Class
Class IIa
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
IT-MF-000029722

Other devices from KW Apparecchi Scientifici Srl

See all devices from KW Apparecchi Scientifici Srl →

Properties

Other properties (13)

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