Invacare® XPO2™ Portable Oxygen Concentrator XPO100BE

GUDID 08414471000223

INVACARE CORPORATION

Mobile/portable oxygen concentrator

• Primary Device ID: 08414471000223
• NIH Device Record Key: 5f4e302a-6dfb-4b36-93b6-0b94f03beb2a
• Commercial Distribution Discontinuation: 2015-11-23
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Invacare® XPO2™ Portable Oxygen Concentrator
• Version Model Number: XPO100BE
• Catalog Number: XPO100BE
• Company DUNS: 076916246
• Company Name: INVACARE CORPORATION
• 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: 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: 440-329-6000
• Email: orders@invacare.com

Operating and Storage Conditions

• Handling Environment Temperature: Between -2 Degrees Fahrenheit and 140 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	08414471000223 [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: 3
• Public Version Date: 2020-04-20
• Device Publish Date: 2015-09-10

On-Brand Devices [Invacare® XPO2™ Portable Oxygen Concentrator]

• 08414471000223: XPO100BE
• 00841447100072: XPO100B
• 00841447100065: XPO100