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Nufix

EUDAMED

Class IIa (EU MDR)

Ref IT-01Model with/without Injection port

by Nubeno Healthcare Private Limited

Identity

Trade Name
NUFIX EUDAMED
Device Name
Peripheral Intravenous Catheter and Cannula (I.V. Cannula) EUDAMED
Model / Reference
with/without Injection port EUDAMED
IT-01 EUDAMED

Identifiers

Primary DI / UDI-DI
89080170180068 EUDAMED
Basic UDI-DI
8908017018IVC015V EUDAMED
EMDN Code
C0101010101 PERIPHERAL I.V. CATHETERS, W/O SAFETY SYSTEMS, WITH INJECTION VALVES EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Nufix by Nubeno Healthcare Private Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED 0f8e8c34-730c-4747-9bda-d6e1acae8e61 61 fields · synced Oct 9, 2026