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Súlyfürdő rozsdamentes acélból, derékővvel, bókasúllyal, ólomsúlyokkal

by DIA-MED Egészségügyi és Gépészeti Berendezéseket Gyártó és Forgalmazó Kft.

Ref FI10

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 Number599957120SU00SX Basic UDI-DI 05999571200344UDI-DIDate28 Mar 2025RegisteredStatusActive

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  • Withdrawn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
Súlyfürdő
Model / Reference
FI10
Primary DI / UDI-DI
05999571200344
Basic UDI-DI
599957120SU00SX
EMDN Code
Z120618 Hydrogymnastics and hydrotherapy systems
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000003115

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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