longway

GUDID 06974283900026

Anhui Longway Medical Technology Co.,Ltd

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06974283900026
• NIH Device Record Key: fce512c4-b2d4-4931-a56a-85ae6d2cf6d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: longway
• Version Model Number: LW01301A07
• Company DUNS: 405785078
• Company Name: Anhui Longway Medical 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: false
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	06974283900026 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K250366

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: 2025-09-04
• Device Publish Date: 2025-08-27