Skip to content

Zestaw wyposażenia kabiny UGUL, PUR

by Kinesis Spółka z ograniczoną odpowiedzialnością 3 variants

Ref OSPRZĘT MAX

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5904347808osprzetRH Basic UDI-DI 05904347808402UDI-DIDate18 Feb 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  • Withdrawn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
Zestaw wyposażenia kabiny UGUL, PUR
Model / Reference
OSPRZĘT MAX
Primary DI / UDI-DI
05904347808402
Basic UDI-DI
5904347808osprzetRH
Direct Marketing DI
05904347808402
EMDN Code
Z120602 Physiotherapy equipment
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000023594

Other devices from Kinesis Spółka z ograniczoną odpowiedzialnością

See all devices from Kinesis Spółka z ograniczoną odpowiedzialnością →

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