EUDAMED device

AIRFIT F30i SYS - M/STD - EU

EUDAMED device 00619498633128 · ResMed PTY LTD

Key facts

Primary DI 00619498633128
Trade name AIRFIT F30i SYS - M/STD - EU
Device name AirFit F30i,AirFit F30i Non Magnetic
Reference or catalog number 63312
Manufacturer ResMed PTY LTD
Manufacturer SRN AU-MF-000011753
Risk class Class IIa
EMDN code R0301010201
EMDN description CPAP MASKS
Legislation mdr
Implantable No
Sterile No
Single use No
Status date Oct 27, 2025

At a glance

  • No Matching FDA GUDID record

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About EUDAMED devices

EUDAMED is the European Union's database of medical devices registered under the MDR and IVDR, including UDI-DIs, risk classes and EMDN nomenclature codes.

Source: European Commission, European Database on Medical Devices (EUDAMED) · Source date:

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