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AirSense 11 AutoSet NORD

EUDAMED

Class IIa (EU MDR)

Ref 39180Ref 39181

by ResMed PTY LTD

Identity

Trade Name
AirSense 11 AutoSet NORD EUDAMED
AirSense 11 AutoSet NORD TRI EUDAMED
Device Name
AirSense 11 AutoSet , AirSense 11 Elite EUDAMED
Model / Reference
39180 EUDAMED
39181 EUDAMED

Identifiers

Primary DI / UDI-DI
00619498391806 EUDAMED
00619498391813 EUDAMED
Basic UDI-DI
619498EC19776 EUDAMED
Direct Marketing DI
00619498394630 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

AirSense 11 AutoSet NORD 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 (2)

  • EUDAMED 5ea2f0af-efa5-4039-9993-100f2fae9064 61 fields · synced Jul 26, 2026
  • EUDAMED 322a2088-3a0b-4537-a41a-e09c5eb87871 61 fields · synced May 16, 2026