FREEDOMCHAIR

GUDID 06971086400180

Kunshan Aoshida Electric Technology Co., Ltd

Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible Wheelchair, electric-motor-driven, attendant-controlled, powered-steering, non-collapsible

• Primary Device ID: 06971086400180
• NIH Device Record Key: 5d63b2a6-c319-470d-865b-00691ba0646e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FREEDOMCHAIR
• Version Model Number: A08L
• Company DUNS: 543600297
• Company Name: Kunshan Aoshida Electric Technology Co., Ltd
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971086400180 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K163204

FDA Product Code

• ITI: Wheelchair, Powered

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: 2022-11-21
• Device Publish Date: 2022-11-12

Devices Manufactured by Kunshan Aoshida Electric Technology Co., Ltd

• 06971086400180 - FREEDOMCHAIR: 2022-11-21
• 06971086400180 - FREEDOMCHAIR: 2022-11-21
• 06971086400012 - FREED MCHVIR: 2018-07-06
• 06971086400029 - FREED MCHVIR: 2018-07-06
• 06971086400036 - FREED MCHVIR: 2018-07-06
• 06971086400043 - FREED MCHVIR: 2018-07-06
• 06971086400050 - FREED MCHVIR: 2018-07-06
• 06971086400067 - FREED MCHVIR: 2018-07-06
• 06971086400074 - FREED MCHVIR: 2018-07-06