ELECTRIC WHEELCHAIR

GUDID 06977027830467

Zhejiang Nysin Medical Co.,Ltd

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06977027830467
• NIH Device Record Key: 2fc157e3-2c6c-48b6-bc03-5cccd10b545c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ELECTRIC WHEELCHAIR
• Version Model Number: NXN20-205
• Company DUNS: 632947785
• Company Name: Zhejiang Nysin Medical 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: true
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com
• Phone: 3038000162
• Email: wm06@chinaqianxi.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	06977027830467 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241379

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: 2024-11-26
• Device Publish Date: 2024-11-18

On-Brand Devices [ELECTRIC WHEELCHAIR ]

• 06977027830467: NXN20-205
• 06977027830481: XFGW25-203