myAir 22246

GUDID 00840193400122

myAir (Android)

RESMED CORP.

Ventilator application software

• Primary Device ID: 00840193400122
• NIH Device Record Key: 3cdc4f5d-02f6-4254-ba9b-799a1c8e95a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: myAir
• Version Model Number: 22246
• Catalog Number: 22246
• Company DUNS: 080243150
• Company Name: RESMED CORP.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 800-424-0737
• Email: reception@resmed.com
• Phone: 800-424-0737
• Email: reception@resmed.com
• Phone: 800-424-0737
• Email: reception@resmed.com
• Phone: 800-424-0737
• Email: reception@resmed.com
• Phone: 800-424-0737
• Email: reception@resmed.com
• Phone: 800-424-0737
• Email: reception@resmed.com
• Phone: 800-424-0737
• Email: reception@resmed.com
• Phone: 800-424-0737
• Email: reception@resmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840193400122 [Primary]

FDA Product Code

• BZD: Ventilator, Non-Continuous (Respirator)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-05
• Device Publish Date: 2021-07-28

On-Brand Devices [myAir]

• 00840193400122: myAir (Android)
• 00840193400115: myAir (iOS)