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Lm-Adult High Flow-Lg

EUDAMED

Class IIa (EU MDR)

Ref LMMD2001

by Foxxmed Ltd

Identity

Trade Name
LM-ADULT HIGH FLOW-LG EUDAMED
Device Name
LM-ADULT HIGH FLOW-LG EUDAMED
Model / Reference
LMMD2001 EUDAMED

Identifiers

Primary DI / UDI-DI
04719876360298 EUDAMED
Basic UDI-DI
B-04719876360298 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

Lm-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

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Manufacturer

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

Sources (1)

  • EUDAMED 9ae49f93-47bc-4c1e-ace6-704e4755dd57 61 fields · synced Jul 9, 2026