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Nufix

by Nubeno Healthcare Private Limited 2 variants

Ref IT212419Model with/without Injection port

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8908017018IVC015V Basic UDI-DI 08908017018204UDI-DIDate9 Sep 2023RegisteredStatusActive

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  • Withdrawn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
Peripheral Intravenous Catheter and Cannula (I.V. Cannula)
Model / Reference
with/without Injection port, IT212419
Primary DI / UDI-DI
08908017018204
Basic UDI-DI
8908017018IVC015V
EMDN Code
C0101010101 Peripheral i.v. catheters, w/o safety systems, with injection valves
Device Class
Class IIa
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
IN-MF-000014550
Authorised representative
EUCEREP B.V. NL-AR-000001966

Other devices from Nubeno Healthcare Private Limited

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Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No