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Airsense 11 Autoset Eu

EUDAMED

Class IIa (EU MDR)

Ref 39153Ref 39154

by ResMed PTY LTD

Identity

Trade Name
AIRSENSE 11 AUTOSET EU EUDAMED
AIRSENSE 11 AUTOSET EU CO EUDAMED
Device Name
AirSense 11 AutoSet , AirSense 11 Elite EUDAMED
Model / Reference
39153 EUDAMED
39154 EUDAMED

Identifiers

Primary DI / UDI-DI
00619498391530 EUDAMED
00619498391547 EUDAMED
Basic UDI-DI
619498EC19776 EUDAMED
Direct Marketing DI
00619498394104 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 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 (2)

  • EUDAMED f0e8ae87-13ab-4fa8-b2e3-1cd622ef849d 61 fields · synced Jul 31, 2026
  • EUDAMED 3dd44529-69c7-43a7-a2e1-52bad63227e0 61 fields · synced May 18, 2026