AILIFEE

GUDID 06953775661232

Alicn Medical Shenzhen, Inc.

Automatic-inflation electronic sphygmomanometer, portable, arm/wrist

• Primary Device ID: 06953775661232
• NIH Device Record Key: 4c5549e7-bb0c-4c5d-8cf2-6ce76b50d4d0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AILIFEE
• Version Model Number: AES-U392
• Company DUNS: 548040741
• Company Name: Alicn Medical Shenzhen, Inc.
• 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: false
• 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	06953775661232 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K231050

FDA Product Code

• DXN: System, Measurement, Blood-Pressure, Non-Invasive

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: 2025-05-27
• Device Publish Date: 2025-05-19

On-Brand Devices [AILIFEE]

• 06953775661263: AES-U632
• 06953775661256: AES-U612
• 06953775661249: AET-R1F1
• 06953775661232: AES-U392
• 06953775661225: AES-U231