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BL650 Kit SUPRA17 Hemox Flexya

by Bellco s.r.l. 2 variants

Ref IB0569211Model BL650

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 Number0763000B00000677E Basic UDI-DI 08032979793197UDI-DIDate15 Oct 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  • Withdrawn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
BL650, IB0569211
Primary DI / UDI-DI
08032979793197
Basic UDI-DI
0763000B00000677E
EMDN Code
F0301 Haemofiltration-haemodiafiltration kits
Device Class
Class IIb
Medical Purpose
Procedure pack for haemodiafiltration therapy with endogenous reinfusion.

Manufacturer details

EUDAMED SRN
IT-PR-000022066

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Properties

Other properties (1)

  • Sterile: No