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Airfit N30 Mask Sys Multihole Eu

EUDAMED

Class IIa (EU MDR)

Ref 64205

by ResMed PTY LTD

Identity

Trade Name
AIRFIT N30 MASK SYS MULTIHOLE EU EUDAMED
Device Name
AirFit N30, AirFit N30 AirMini EUDAMED
Model / Reference
64205 EUDAMED

Identifiers

Primary DI / UDI-DI
00619498642052 EUDAMED
Basic UDI-DI
619498EC18773 EUDAMED
Direct Marketing DI
00619498004171 EUDAMED
EMDN Code
R0301010201 CPAP MASKS 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

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

Airfit N30 Mask Sys Multihole Eu by Resmed Pty Ltd — 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

Manufacturer
ResMed PTY LTD
EUDAMED SRN
AU-MF-000011753
Authorised Representative
ResMed SAS FR-AR-000007151

Sources (1)

  • EUDAMED dc3a1933-614f-4486-9457-f50a3c4cd3ea 61 fields · synced Jun 18, 2026