Skip to content

Komora do suchych kąpieli w dwutlenku węgla lub ozonie DUO DRY JET

by Biuro Handlowe Kinesis Andrzej Boruta

Ref Duo Dry JetModel DUO DRY JET

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05904063815432 Basic UDI-DI 05904063815432UDI-DIDate24 Nov 2023RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Komora do suchych kąpieli w dwutlenku węgla lub ozonie DUO DRY JET
Model / Reference
DUO DRY JET
Primary DI / UDI-DI
05904063815432
Basic UDI-DI
B-05904063815432
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class IIa
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000018445

Other devices from Biuro Handlowe Kinesis Andrzej Boruta

See all devices from Biuro Handlowe Kinesis Andrzej Boruta →

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