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Sp-Infant High Flow-M

EUDAMED

Class IIa (EU MDR)

Ref SPMD2033

by Foxxmed Ltd

Identity

Trade Name
SP-INFANT HIGH FLOW-M EUDAMED
Device Name
SP-INFANT HIGH FLOW-M EUDAMED
Model / Reference
SPMD2033 EUDAMED

Identifiers

Primary DI / UDI-DI
04719876360946 EUDAMED
Basic UDI-DI
B-04719876360946 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

Sp-Infant High Flow-M 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 ce382c66-d874-400c-91ba-9605a59d3a91 61 fields · synced Jul 25, 2026