Invacare® MyOn™ Ultralightweight Folding Wheelchair MYONTS

GUDID 00841447102502

Invacare® MyOn™ Ultralightweight Folding Wheelchair

INVACARE CORPORATION

Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible

• Primary Device ID: 00841447102502
• NIH Device Record Key: 79de6969-dd7a-473f-8a2d-e0d27c30746e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Invacare® MyOn™ Ultralightweight Folding Wheelchair
• Version Model Number: MYONTS
• Catalog Number: MYONTS
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(440)329-6000
• Email: orders@invacare.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841447102502 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K930803

FDA Product Code

• IOR: Wheelchair, mechanical

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: 2019-06-18
• Device Publish Date: 2019-06-10

On-Brand Devices [Invacare® MyOn™ Ultralightweight Folding Wheelchair]

• 00841447102502: Invacare® MyOn™ Ultralightweight Folding Wheelchair
• 00841447102441: Invacare® MyOn™ Ultralightweight Folding Wheelchair