← Back to catalogue

Fm-Adult High Flow-Lg

EUDAMED

Class IIa (EU MDR)

Ref FMMD2001

by Foxxmed Ltd

Identity

Trade Name
FM-ADULT HIGH FLOW-LG EUDAMED
Device Name
FM-ADULT HIGH FLOW-LG EUDAMED
Model / Reference
FMMD2001 EUDAMED

Identifiers

Primary DI / UDI-DI
04719876360007 EUDAMED
Basic UDI-DI
B-04719876360007 EUDAMED
EMDN Code
R0301020302 HIGH FLOW THERAPY NASAL CANNULAS (HFNC) 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

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Fm-Adult High Flow-Lg by Foxxmed Ltd — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Foxxmed Ltd
EUDAMED SRN
TW-MF-000022145
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED b8352d64-9e88-4545-a302-cf25cd9d0809 61 fields · synced Jun 19, 2026