eudamed_udi
Primary ID: 06953775662161
AILIFEE (UDI 06953775662161)
Manufactured by Alicn Medical Shenzhen, Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AILIFEE - Primary ID 06953775662161
Device Regulatory Overview
The AILIFEE (Model/Catalog Number: AES-U512) is a medical device manufactured by Alicn Medical Shenzhen, Inc. This product is indexed under FDA Product Code / Category Classification Z1203020302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AES-U512
- Product Code / EMDN
- Z1203020302
- Device Name
- Arm Blood Pressure Monitor
- Database Sync Date
- 2026-08-09 16:29:11
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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Get API Token Access ($49/mo)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 06953775662161.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020302.
Similar Classification Devices (Z1203020302)
Other Devices by Alicn Medical Shenzhen, Inc
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