gudid
Primary ID: AES-U632
BBLOVE (UDI AES-U632)
Manufactured by Alicn Medical Shenzhen, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BBLOVE - Primary ID AES-U632
Device Regulatory Overview
The BBLOVE (Model/Catalog Number: AES-U632) is a medical device manufactured by Alicn Medical Shenzhen, Inc.. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AES-U632
- Product Code / EMDN
- DXN
- 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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BBLOVE?
The registered manufacturer of record for BBLOVE is Alicn Medical Shenzhen, Inc..
What is the Primary UDI-DI identifier for BBLOVE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AES-U632.
What classification code is assigned to this device?
This device is registered under product classification code DXN.
Similar Classification Devices (DXN)
Other Devices by Alicn Medical Shenzhen, Inc.
Programmatic Export
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