eudamed_udi
Primary ID: 06971354100682
ReLIA (UDI 06971354100682)
Manufactured by ReLIA Biotechnologies (Jiangsu), Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ReLIA - Primary ID 06971354100682
Device Regulatory Overview
The ReLIA (Model/Catalog Number: RG16237-50T) is a medical device manufactured by ReLIA Biotechnologies (Jiangsu), Inc.. This product is indexed under FDA Product Code / Category Classification W01021109 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RG16237-50T
- Product Code / EMDN
- W01021109
- Device Name
- Full-Scale C-Reactive Protein Test (CRP) (Colloidal Gold)
- Database Sync Date
- 2026-08-09 16:50:06
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 ReLIA?
The registered manufacturer of record for ReLIA is ReLIA Biotechnologies (Jiangsu), Inc..
What is the Primary UDI-DI identifier for ReLIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971354100682.
What classification code is assigned to this device?
This device is registered under product classification code W01021109.
Similar Classification Devices (W01021109)
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