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NephroNeedle

by Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇ 31 variants

Ref 4218307Model NephroNeedle15VSE

NephroNeedle (4218307) is a Class IIa device made by Nephrocan Medi̇kal Sanayi̇ Ti̇caret Anoni̇m Şi̇rketi̇, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-868475920302PA), 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-868475920302PA Basic UDI-DI D-868475920302PAUDI-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  • Withdrawn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
Fistula Needle for Hemodialysis
Model / reference
NephroNeedle15VSE, 4218307
Primary DI / UDI-DI
D-868475920302PA
Basic UDI-DI
B-868475920302PA
EMDN code
A010401 Arteriovenous fistula 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 FISTULA 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)