Skip to content

Fotel zabiegowy

by Kinesis Spółka z ograniczoną odpowiedzialnością Poland EUDAMED

Ref FZ-K EMDN V08020199

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5904347808fotelZW Basic UDI-DIDate16 Feb 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Fotel zabiegowy
Model / Reference
FZ-K
Primary DI / UDI-DI
05905178376368
Basic UDI-DI
5904347808fotelZW
Direct Marketing DI
05905178376368
EMDN Code
V08020199 Electric medical chairs - other
Device Class
Class I
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 & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 1243d16c-c7c3-4d70-9bfa-8482da279a1b 61 fields · synced 22 Oct 2026