Mobi

GUDID 09353645350018

Mobi AMER1 (AMO)

RESMED ASIA PTE. LTD.

Mobile/portable oxygen concentrator

• Primary Device ID: 09353645350018
• NIH Device Record Key: 0c9ad12b-ec2c-4ed9-9c47-78da27bf13c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mobi
• Version Model Number: 35001
• Company DUNS: 659276906
• Company Name: RESMED ASIA PTE. LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• 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: 800-427-0737
• Email: reception@resmed.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 60 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	09353645350018 [Primary]

FDA Product Code

• CAW: Generator, Oxygen, Portable

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-20
• Device Publish Date: 2018-07-27

On-Brand Devices [Mobi]

• 09353645350018: Mobi AMER1 (AMO)
• 09353645000562: Mobi - Refurbished