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Bomboletta da 10 litri - NO pescante

by Nippon Sanso Pharma S.r.l.

Ref 9CDOO4HBModel FT51 - CO2

Active European Union

CE MDR

Valid until

23 Sep 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier CERTIQUALITY S.r.l.

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 Number805979322FT51CO2L7 Basic UDI-DI 08059793220302UDI-DIDate7 Oct 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 58866 Active

    Quality management system EU MDR

    Certifier
    CERTIQUALITY S.r.l. 0546
    Issued
    24 Sep 2026
    Expires
    23 Sep 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Anidride carbonica per crioterapia in chirurgia come fluido per il funzionamento di apparecchiature specifiche quali sistemi spray o stick
Model / Reference
FT51 - CO2, 9CDOO4HB
Primary DI / UDI-DI
08059793220302
Basic UDI-DI
805979322FT51CO2L7
Direct Marketing DI
08059793220302
EMDN Code
V0901 Clinical/therapeutic applications carbon dioxide
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000029403

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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