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Ppj-20 Hallux Valgus Kezelő /Jobb/S/35-36

by PRIMA-PROTETIKA Gyártó és Kereskedelmi Korlátolt Felelősségű Társaság

Ref 200616220P135Model PPJ-20 HALLUX VALGUS KEZELŐ

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 Number59989941PPTALP-0114-LL Basic UDI-DI 05998994162208UDI-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  • Withdrawn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
PPJ-20 HALLUX VALGUS KEZELŐ, 200616220P135
Primary DI / UDI-DI
05998994162208
Basic UDI-DI
59989941PPTALP-0114-LL
EMDN Code
Y06120602 Energy return ankle-foot orthoses
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