eudamed_udi
Primary ID: 06974754670113
Alliment (UDI 06974754670113)
Manufactured by Beijing Bonsci Technology Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alliment - Primary ID 06974754670113
Device Regulatory Overview
The Alliment (Model/Catalog Number: A000202) is a medical device manufactured by Beijing Bonsci Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification P099001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A000202
- Product Code / EMDN
- P099001
- Device Name
- Orthopaedic Cements
- Database Sync Date
- 2026-08-09 16:58:20
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 Alliment?
The registered manufacturer of record for Alliment is Beijing Bonsci Technology Co., Ltd..
What is the Primary UDI-DI identifier for Alliment?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974754670113.
What classification code is assigned to this device?
This device is registered under product classification code P099001.
Similar Classification Devices (P099001)
Other Devices by Beijing Bonsci Technology Co., Ltd.
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