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Nikinox

EUDAMED

Class I (EU MDR)

Ref 010092Model NIKI2002

by Airnova Srl

Identity

Trade Name
NIKINOX EUDAMED
Device Name
SISTEMA DI EVACUAZIONE MOBILE A DOPPIA MASCHERA NIKI2002 EUDAMED
Model / Reference
NIKI2002 EUDAMED
010092 EUDAMED

Identifiers

Primary DI / UDI-DI
08055304120017 EUDAMED
Basic UDI-DI
805530412NIKIA5 EUDAMED
Direct Marketing DI
08055304120017 EUDAMED
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

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

Category: Pulmonary function analysis system, adult

Nikinox by Airnova Srl — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function analysis system, adult.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Airnova Srl
EUDAMED SRN
IT-MF-000011251

Sources (1)

  • EUDAMED 3dc25c91-216a-473d-b9dc-62183925dd9b 61 fields · synced Jul 14, 2026