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AirCurve 10 CS PaceWave DE CO

EUDAMED

Class IIa (EU MDR)

Ref 37278

by ResMed PTY LTD

Identity

Trade Name
AirCurve 10 CS PaceWave DE CO EUDAMED
Device Name
AirCurve 10 CS PaceWave EUDAMED
Model / Reference
37278 EUDAMED

Identifiers

Primary DI / UDI-DI
00619498372782 EUDAMED
Basic UDI-DI
619498EC1516E EUDAMED
Direct Marketing DI
00619498371389 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

AirCurve 10 CS PaceWave 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 ad81f236-feae-44d7-b417-4e3c73a58920 61 fields · synced Jul 26, 2026