AILIFEE

GUDID 06953775662086

Alicn Medical Shenzhen, Inc.

Intermittent electronic patient thermometer

• Primary Device ID: 06953775662086
• NIH Device Record Key: 291dfd25-55ec-49f1-acef-7d873c020302
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AILIFEE
• Version Model Number: AET-F371
• 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	06953775662086 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K232338

FDA Product Code

• SDV: Clinical Electronic Thermometer

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2026-02-05
• Device Publish Date: 2025-11-19

On-Brand Devices [AILIFEE]

• 06953775661263: AES-U632
• 06953775661256: AES-U612
• 06953775661249: AET-R1F1
• 06953775661232: AES-U392
• 06953775661225: AES-U231
• 06953775661638: AET-F355
• 06953775661621: AET-F372
• 06953775661614: AET-R832
• 06953775661607: AET-R171
• 06953775661591: AES-U312
• 06953775661584: AES-U181
• 06953775662055: AET-F101
• 06953775662086: AET-F371
• 06953775662253: AES-U522
• 06953775662246: AET-F221