AILIFEE (UDI AET-F355)

Manufactured by Alicn Medical Shenzhen, Inc.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The AILIFEE (Model/Catalog Number: AET-F355) is a medical device manufactured by Alicn Medical Shenzhen, Inc.. This product is indexed under FDA Product Code / Category Classification FLL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AET-F355
Product Code / EMDN: FLL
Device Name
Database Sync Date: 2026-08-09 09:05:25

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of AILIFEE?

The registered manufacturer of record for AILIFEE is Alicn Medical Shenzhen, Inc..

What is the Primary UDI-DI identifier for AILIFEE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AET-F355.

What classification code is assigned to this device?

This device is registered under product classification code FLL.

Similar Classification Devices (FLL)

Other Devices by Alicn Medical Shenzhen, Inc.

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