myAir

FDA UDI

Class II (US FDA UDI)

by Resmed Corp

Identity

Trade Name: myAir FDA UDI
Generic Name: Self-care monitoring/reporting software FDA UDI
Device Name: myAir (Android) FDA UDI
Model / Reference: 22246 FDA UDI
Description: myAir (Android) FDA UDI

Identifiers

Catalog Number: 22246 FDA UDI
Primary DI / UDI-DI: 00840193400122 FDA UDI
FDA Product Code: BZD FDA UDI
MNR FDA UDI
GMDN Term: Self-care monitoring/reporting software FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5905 FDA UDI
868.2375 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Self-care monitoring/reporting software

myAir by Resmed Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Resmed Corp

Sources (1)

FDA UDI 3cdc4f5d-02f6-4254-ba9b-799a1c8e95a1 35 fields · synced Jun 8, 2026