Insulin FIA Kit (UDI 06974674892312)
Manufactured by Shenzhen Zijian Biotechnology Co., Ltd
Device Regulatory Overview
The Insulin FIA Kit (Model/Catalog Number: 18-02-0061) is a medical device manufactured by Shenzhen Zijian Biotechnology Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102060103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 18-02-0061
- Product Code / EMDN
- W0102060103
- Device Name
- Insulin FIA Kit
- Database Sync Date
- 2026-08-09 16:46:20
Full Regulatory Attributes
π Token Gated
{
"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 Insulin FIA Kit?
The registered manufacturer of record for Insulin FIA Kit is Shenzhen Zijian Biotechnology Co., Ltd.
What is the Primary UDI-DI identifier for Insulin FIA Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974674892312.
What classification code is assigned to this device?
This device is registered under product classification code W0102060103.
Similar Classification Devices (W0102060103)
Other Devices by Shenzhen Zijian Biotechnology Co., Ltd
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