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Azoto Dm Sico

by SICO Società Italiana Carburo Ossigeno S.p.A. EUDAMED

Active European Union

Ref DMAZOXXRD01C02500ZNZ

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805948259N201EV Basic UDI-DIDate14 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • EPT 0477.MDR.22/4850.2 Reissued

    Quality management system EU MDR

    Notified body
    Notified body 0477
    Issued
    7 Apr 2026
    Expires
    13 Jun 2027

Specification

EUDAMED

Device Name
Azoto Dm Sico
Model / Reference
DMAZOXXRD01C02500ZNZ
Primary DI / UDI-DI
08059482591119
Basic UDI-DI
805948259N201EV
Direct Marketing DI
08059482590846
EMDN Code
V0902 Clinical/therapeutic applications liquid nitrogen
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000028343

Other devices from SICO Società Italiana Carburo Ossigeno S.p.A.

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Properties

Show 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