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Airview

FDA UDI

Class II (US FDA UDI)

by Resmed Corp

Identity

Trade Name
AIRVIEW FDA UDI
Generic Name
Ventilator application software FDA UDI
Device Name
AIRVIEW FDA UDI
Model / Reference
22240 FDA UDI
Description
AIRVIEW FDA UDI

Identifiers

Catalog Number
22240 FDA UDI
Primary DI / UDI-DI
00619498222407 FDA UDI
FDA Product Code
MNS FDA UDI
MNR FDA UDI
CBK FDA UDI
BZD FDA UDI
GMDN Term
Ventilator application software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
868.2375 FDA UDI
868.5905 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ventilator application software

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

Similar devices

Also classified as Ventilator application software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Resmed Corp

Sources (1)

  • FDA UDI 06781baf-ee82-4ec8-b4f3-6720deb9bf06 35 fields · synced Jun 8, 2026