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H4i for Stellar FRANCE

EUDAMED

Class IIa (EU MDR)

Ref 24936

by ResMed PTY LTD

Identity

Trade Name
H4i for Stellar FRANCE EUDAMED
Device Name
H4i EUDAMED
Model / Reference
24936 EUDAMED

Identifiers

Primary DI / UDI-DI
00619498249367 EUDAMED
Basic UDI-DI
B-00619498249367 EUDAMED
EMDN Code
Z1203019080 VARIOUS INSTRUMENTS FOR ANAESTHESIA AND PULMONARY VENTILATION SUPPORT - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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

H4i for Stellar FRANCE by Resmed Pty 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
ResMed PTY LTD
EUDAMED SRN
AU-MF-000011753
Authorised Representative
ResMed SAS FR-AR-000007151

Sources (1)

  • EUDAMED b7c7c1a0-9b90-4e74-883b-d4a50e53bae2 61 fields · synced Jul 12, 2026