Solax

GUDID 06970990830519

Electric wheelchair

Guangdong Prestige Technology Co., Ltd.

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06970990830519
• NIH Device Record Key: 3e055099-421a-4205-8f24-f72ad1eebd37
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Solax
• Version Model Number: S7018
• Company DUNS: 529507263
• Company Name: Guangdong Prestige Technology Co., 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: false
• Serial Number: true
• Manufacturing Date: false
• 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	06970990830519 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K240270

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: 2024-09-23
• Device Publish Date: 2024-09-13