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Biztonsági Öv Kerekesszékhez K2 4CSATTOS

by PRIMA-PROTETIKA Gyártó és Kereskedelmi Korlátolt Felelősségű Társaság

Ref 2008395006000Model BIZTONSÁGI ÖV KEREKESSZÉKHEZ K2

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59989941PPKEREKES-0282-GG Basic UDI-DI 05998994151981UDI-DIDate30 Sep 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  • Withdrawn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

Model / Reference
BIZTONSÁGI ÖV KEREKESSZÉKHEZ K2, 2008395006000
Primary DI / UDI-DI
05998994151981
Basic UDI-DI
59989941PPKEREKES-0282-GG
EMDN Code
Y122406 Belts, seats and armrests for wheelchairs
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000003677

Other devices from PRIMA-PROTETIKA Gyártó és Kereskedelmi Korlátolt Felelősségű Társaság

See all devices from PRIMA-PROTETIKA Gyártó és Kereskedelmi Korlátolt Felelősségű Társaság →

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