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08681546490627-RF-A43G Asidik Konsantre Hemodiyaliz Solüsyonu 10 litre 1:45

by Reos Tibbi̇ Ci̇hazlar Ltd. Şti̇.

Ref 08681546490627-RF-A43GModel RF-A43G ASİDİK KONSTRE HEMODİYALİZ SOLÜSYONU 10 Litre % 45

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08681546490627 Basic UDI-DI 08681546490627UDI-DIDate12 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Rf-A43G Asi̇di̇k Konstre Hemodi̇yali̇z Solüsyonu (10 Lt)
Model / Reference
RF-A43G ASİDİK KONSTRE HEMODİYALİZ SOLÜSYONU 10 Litre % 45, 08681546490627-RF-A43G
Primary DI / UDI-DI
08681546490627
Basic UDI-DI
B-08681546490627
EMDN Code
F040101 Dialysis concentrates, acid solutions, non-sterile
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000018678

Other devices from Reos Tibbi̇ Ci̇hazlar Ltd. Şti̇.

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