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Cryogen Canister

by Cynosure Lutronic Technology Corporation

Ref LUT-ICD 550A

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88002918211011aJK Basic UDI-DI 08800291821757UDI-DIDate21 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Cryogen Canister
Model / Reference
LUT-ICD 550A
Primary DI / UDI-DI
08800291821757
Basic UDI-DI
88002918211011aJK
EMDN Code
Z12010985 Electrosurgery instruments - consumables
Device Class
Class I
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
KR-MF-000047499
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Cynosure Lutronic Technology Corporation

See all devices from Cynosure Lutronic Technology Corporation →

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