ReLIA (UDI 06971354101900)
Manufactured by ReLIA Biotechnologies (Jiangsu), Inc.
Device Regulatory Overview
The ReLIA (Model/Catalog Number: RF16387-50T) is a medical device manufactured by ReLIA Biotechnologies (Jiangsu), Inc.. This product is indexed under FDA Product Code / Category Classification W0101060107 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RF16387-50T
- Product Code / EMDN
- W0101060107
- Device Name
- Glycosylated Hemoglobin (HbA1c) Assay Kit (Fluorescence Immunoassay)
- Database Sync Date
- 2026-08-09 16:44:57
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 06971354101900.
What classification code is assigned to this device?
This device is registered under product classification code W0101060107.
Similar Classification Devices (W0101060107)
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