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AirCurve 10 S DE CO

EUDAMED

Class IIa (EU MDR)

Ref 37251

by ResMed PTY LTD

Identity

Trade Name
AirCurve 10 S DE CO EUDAMED
Device Name
AirCurve 10 S, AirCurve 10 ST, AirCurve 10 VAuto EUDAMED
Model / Reference
37251 EUDAMED

Identifiers

Primary DI / UDI-DI
00619498372515 EUDAMED
Basic UDI-DI
619498EC1506C EUDAMED
Direct Marketing DI
00619498371327 EUDAMED
EMDN Code
Z12030102 CONTINUOUS POSITIVE PRESSURE EQUIPMENT 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

Yes

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

AirCurve 10 S DE CO 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 1ce190aa-3c34-4e2e-b7b8-3deaad054d88 61 fields · synced Jun 18, 2026