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Krzesło do masażu Flexo biały k501

by HABYS Sp. z o.o.

Ref V-KFLEX001, V-KFLEX003Model Krzesło do masażu Flexo biały k501

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number590666749KrzeslaFA Basic UDI-DI Date30 Mar 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  • Withdrawn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

Trade Name
Krzesło do masażu Flexo biały k501
Krzesło do masażu Flexo -gray
Device Name
Krzesła do masażu
Model / Reference
Krzesło do masażu Flexo biały k501, V-KFLEX001, V-KFLEX003
Primary DI / UDI-DI
05906667493054, 05906667493078
Basic UDI-DI
590666749KrzeslaFA
Direct Marketing DI
05906667493054
05906667493078
EMDN Code
V080202 Manual medical chairs
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000007133

Other devices from HABYS Sp. z o.o.

See all devices from HABYS Sp. z o.o. →

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