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NephroLine

by Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ 14 variants

Ref 4212408Model NephroLineB - B001

NephroLine (4212408) is a Class IIa device made by Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI B-868475920207PF), 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-868475920207PF Basic UDI-DI D-868475920207PFUDI-DIDate4 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Blood tubing sets for hemodialysis (Blood lines)
Model / reference
NephroLineB - B001, 4212408
Primary DI / UDI-DI
D-868475920207PF
Basic UDI-DI
B-868475920207PF
EMDN code
F020102 Arteriovenous dialysis lines, two needles
Device class
Class IIa
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 ARTERIOVENOUS DIALYSIS LINES, TWO NEEDLES.

Other devices from Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇

See all devices from Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ →

Properties

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