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Argon med. Messer 15, 3m3 F50 P300

by Messer Tatragas, spol. s r.o. 2 variants

Ref 101103504Model Argon med. Messer 15,3m3 F50 P300

Active European Union

CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08588008665336 Basic UDI-DI Date6 Apr 2023RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Argón med. Messer 15,3m3 F50 P300
Model / Reference
101103504, Argon med. Messer 15, 3m3 F50 P300
Primary DI / UDI-DI
08588008665336, 08588008665350
Basic UDI-DI
B-08588008665336, B-08588008665350
EMDN Code
V0905 Clinical/therapeutic applications argon
Device Class
Class I
EU market of registration
Slovakia
Poland

Manufacturer details

EUDAMED SRN
SK-MF-000027886

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Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No