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High-flow nasal cannula Respiratory humidifier

EUDAMED

Class IIa (EU MDR)

Ref ACTIVE VE N TILATION HUMIDIFICATION S Y STEMSModel HF3

by Northern Meditec Limited

Identity

Trade Name
High-flow nasal cannula Respiratory humidifier EUDAMED
Device Name
High-Flow Nasal Cannula Respiratory Humidifier EUDAMED
Model / Reference
HF3 EUDAMED
ACTIVE VE N TILATION HUMIDIFICATION S Y STEMS EUDAMED

Identifiers

Primary DI / UDI-DI
06927116600280 EUDAMED
Basic UDI-DI
06927116600000HF39V EUDAMED
Direct Marketing DI
06927116600280 EUDAMED
EMDN Code
R060201 ACTIVE VENTILATION HUMIDIFICATION SYSTEMS, EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

High-flow nasal cannula Respiratory humidifier by Northern Meditec 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
CN-MF-000013521
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (1)

  • EUDAMED 7a8abaf0-422a-4d93-bab0-f012ad53ad25 61 fields · synced Jul 22, 2026