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CryalJet Maxi

by Cortex Technology Aps

Ref E0300102

CryalJet Maxi (E0300102) is a medical device (EU MDR Class IIa; EMDN category cryosurgery equipment) made by Cortex Technology Aps, registered in EUDAMED on 19 Feb 2025 (Basic UDI-DI 5710188020018E), 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 Number5710188020018E Basic UDI-DI 05710188020039UDI-DIDate19 Feb 2025RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
CryoPro Maxi
Model / reference
E0300102
Primary DI / UDI-DI
05710188020039
Basic UDI-DI
5710188020018E
Direct marketing DI
05710188020039
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

Similar devices in this category

Other devices filed under CRYOSURGERY EQUIPMENT.

Other devices from Cortex Technology Aps

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Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)