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Farmakon a 1K 138NA 3AS 8LT

by KON-MED Sağlık İnşaat Turizm ve Eğitim Ltd. Şti. EUDAMED

Active European Union

Ref 510

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8699459938761PX Basic UDI-DIDate12 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2975-MED-2616201 Issued

    Quality management system EU MDR

    Notified body
    Notified body 2975
    Issued
    11 Jun 2026
    Expires
    10 Jun 2031

Specification

EUDAMED

Device Name
Farmakon Acidic Concentrate Hemodialysis Solution
Model / Reference
510
Primary DI / UDI-DI
08699459935104
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000020885

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