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NephroFilter

by Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ 28 variants

Ref 4210269Model NephroPS170R

NephroFilter (4210269) is a Class IIb device made by Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-868475920004NX), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-868475920004NX Basic UDI-DI D-868475920004NXUDI-DIDate6 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Hollow Fiber Hemodialyzer
Model / reference
NephroPS170R, 4210269
Primary DI / UDI-DI
D-868475920004NX
Basic UDI-DI
B-868475920004NX
EMDN code
F01060303 DIALYSERS - UFC > 35 ml/h/mmHg, SYNTHETIC MEMBRANES
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000046244

Similar devices in this category

Other devices filed under DIALYSERS - UFC > 35 ml/h/mmHg, SYNTHETIC MEMBRANES.

Other devices from Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇

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Properties

  • Supplied sterile
Other properties (11, all answered No)