Automated ECLImmunoassay Analyzer (UDI 06978139070765)
Manufactured by Shenzhen Lifotronic Technology Co., Ltd.
Device Regulatory Overview
The Automated ECLImmunoassay Analyzer (Model/Catalog Number: 012130202) is a medical device manufactured by Shenzhen Lifotronic Technology 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
- 012130202
- Product Code / EMDN
- W0201020102
- Device Name
- Automated ECLImmunoassay Analyzer
- Database Sync Date
- 2026-08-09 17:35:41
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 Automated ECLImmunoassay Analyzer?
The registered manufacturer of record for Automated ECLImmunoassay Analyzer is Shenzhen Lifotronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for Automated ECLImmunoassay Analyzer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978139070765.
What classification code is assigned to this device?
This device is registered under product classification code W0201020102.
Similar Classification Devices (W0201020102)
Other Devices by Shenzhen Lifotronic Technology Co., Ltd.
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