Skip to content

Nitrógeno líquido Producto Sanitario (PS) para criopreservación (GNIP2)

by Nippon Sanso Portugal 21 variants

Ref LE-LD12Model GNIP2

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 Number5600791698GNIP277 Basic UDI-DI 05600791698070UDI-DIDate12 Jan 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  • Withdrawn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

Device Name
Azoto Líquido PS para Criopreservação
Model / Reference
GNIP2, LE-LD12
Primary DI / UDI-DI
05600791698070
Basic UDI-DI
5600791698GNIP277
Direct Marketing DI
05600791698070
EMDN Code
V0902 Clinical/therapeutic applications liquid nitrogen
Device Class
Class IIa
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000004891

Other devices from Nippon Sanso Portugal

See all devices from Nippon Sanso Portugal →

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