Identity
- Trade Name
- AirMini app FDA UDI
- Generic Name
- Ventilator application software FDA UDI
- Device Name
- Android FDA UDI
- Model / Reference
- 22244 FDA UDI
- Description
- Android FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00619498222445 FDA UDI
- FDA Product Code
- BZD FDA UDI
- GMDN Term
- Ventilator application software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5905 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ventilator application software
AirMini app by Resmed Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ventilator application software.
- AIRVIEW — Resmed Corp · Class II
- Puritan Bennett — Covidien LP · Class II
- RMDpulse — Resmed Corp · Class II
- AirView — Resmed Corp · Class II
- Puritan Bennett — Covidien LP · Class II
- ResScan — Resmed Corp · Class II
- EasyCare Tx — Resmed Corp · Class II
- AirView — Resmed Corp · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Resmed Pty Ltd
Sources (1)
- FDA UDI 92c0f533-2a74-45c0-accb-55b1bcbf6a64 34 fields · synced May 30, 2026