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NIFI Set

by Sengewald Klinikprodukte GmbH

Ref 6684469-18Model 66731226-02

Active European Union

CE MDR

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4034393CPTURO2A6C Basic UDI-DI 04034393661247UDI-DIDate8 May 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Nefrostomibytesset Norrköping
Model / Reference
66731226-02, 6684469-18
Primary DI / UDI-DI
04034393661247
Basic UDI-DI
4034393CPTURO2A6C
EMDN Code
A019013 Percutaneous needles
Device Class
Class IIa
Medical Purpose
Sterile, disposable procedure pack, combination of devices for disease treatment related to urology.

Manufacturer details

EUDAMED SRN
DE-PR-000020748

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Properties

  • Sterile