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CryoPro Liquid Nitrogen Filter

by Cortex Technology Aps

Ref LNF

CryoPro Liquid Nitrogen Filter (LNF) is a medical device (EU MDR Class IIa; EMDN category cryosurgery equipment) made by Cortex Technology Aps, registered in EUDAMED on 6 May 2026 (Basic UDI-DI 5710188FILTERUD), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5710188FILTERUD Basic UDI-DI 05710188020770UDI-DIDate6 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
LNF
Primary DI / UDI-DI
05710188020770
Basic UDI-DI
5710188FILTERUD
EMDN code
Z120102 Cryosurgery equipment
Device class
Class IIa
EU registration type
Standard device
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
DK-MF-000002984

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Properties

Other properties (14, all answered No)