eudamed_udi
Primary ID: 06973861680282
Anbio (UDI 06973861680282)
Manufactured by Anbio (Xiamen) Biotechnology Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anbio - Primary ID 06973861680282
Device Regulatory Overview
The Anbio (Model/Catalog Number: ADL-i1910) is a medical device manufactured by Anbio (Xiamen) Biotechnology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0201020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ADL-i1910
- Product Code / EMDN
- W0201020102
- Device Name
- Automatic Luminescence Immunoassay Analyzer
- Database Sync Date
- 2026-08-09 16:28:55
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 Anbio?
The registered manufacturer of record for Anbio is Anbio (Xiamen) Biotechnology Co.,Ltd..
What is the Primary UDI-DI identifier for Anbio?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973861680282.
What classification code is assigned to this device?
This device is registered under product classification code W0201020102.
Similar Classification Devices (W0201020102)
Other Devices by Anbio (Xiamen) Biotechnology Co.,Ltd.
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