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Humidair11 Cleanable Row

EUDAMED

Class IIa (EU MDR)

Ref 39112

by ResMed PTY LTD

Identity

Trade Name
HUMIDAIR11 CLEANABLE ROW EUDAMED
Device Name
HumidAir , HumidAir 11 EUDAMED
Model / Reference
39112 EUDAMED

Identifiers

Primary DI / UDI-DI
00619498391127 EUDAMED
Basic UDI-DI
619498EC1856X EUDAMED
Direct Marketing DI
00619498003549 EUDAMED
EMDN Code
Z1203019080 VARIOUS INSTRUMENTS FOR ANAESTHESIA AND PULMONARY VENTILATION SUPPORT - HARDWARE ACCESSORIES 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

Humidair11 Cleanable Row 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 dcfa2f0a-f446-4f86-aa56-9cc8e201eb42 61 fields · synced Jul 14, 2026