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KRIO Intézet Zrt. köldökzsinórvér és placenta eredetű köldökzsinórvér gyűjtőszett

by KRIO Intézet Sejt- és Szövetbank Zrt.

Ref 5999888040213, 5999888040206

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59998880402KRIOCB0000HH Basic UDI-DI Date20 Dec 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Trade Name
KRIO Intézet Zrt. köldökzsinórvér és placenta eredetű köldökzsinórvér gyűjtőszett
KRIO Intézet Zrt. köldökzsinórvér gyűjtőszett
Model / Reference
5999888040213, 5999888040206
Primary DI / UDI-DI
05999888040213, 05999888040206
Basic UDI-DI
59998880402KRIOCB0000HH
EMDN Code
B0105 Umbilical cord blood collection, purification, cryopreservation bags and kits
Device Class
Class I
Medical Purpose
Köldökzsinórvér gyűjtőszett

Manufacturer details

EUDAMED SRN
HU-PR-000020843

Other devices from KRIO Intézet Sejt- és Szövetbank Zrt.

Properties

Other properties (1)

  • Sterile: No