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DIASOL K2GAc2 ACIDIC BICARBONATE HEMODIALYSIS SOLUTION

by Farmasol Tibbi̇ Ürünler San. Ve Ti̇c. A.Ş. EUDAMED

Active European Union

Ref DIASOL K2GAc2Model DIASOL K2GAc2 -5LT

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08697658010042 Basic UDI-DIDate15 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Acidic Bicarbonate Hemodialysis Solution
Model / Reference
DIASOL K2GAc2 -5LT, DIASOL K2GAc2
Primary DI / UDI-DI
08697658010042
Basic UDI-DI
B-08697658010042
EMDN Code
F040101 Dialysis concentrates, acid solutions, non-sterile
Device Class
Class IIb
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000018494

Other devices from Farmasol Tibbi̇ Ürünler San. Ve Ti̇c. A.Ş.

See all devices from Farmasol Tibbi̇ Ürünler San. Ve Ti̇c. A.Ş. →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No