Nanjing Kangni Smart Technology Co., Ltd.

GUDID 06972665816019

Nanjing Kangni Smart Technology Co., Ltd.

Electric-motor-driven wheelchair, occupant-controlled

• Primary Device ID: 06972665816019
• NIH Device Record Key: 9a0d50ad-506f-497a-8539-0acbb5db0205
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nanjing Kangni Smart Technology Co., Ltd.
• Version Model Number: KZ301B
• Company DUNS: 544542471
• Company Name: Nanjing Kangni Smart 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: true
• 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	06972665816019 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K252494

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: 2026-02-19
• Device Publish Date: 2026-02-11

On-Brand Devices [Nanjing Kangni Smart Technology Co., Ltd.]

• 06972665816019: KZ301B
• 06972665816002: KD101