Cortisol Test (FIA) (UDI 06978139071380)
Manufactured by Shenzhen Lifotronic Technology Co., Ltd.
Device Regulatory Overview
The Cortisol Test (FIA) (Model/Catalog Number: 0320307202) is a medical device manufactured by Shenzhen Lifotronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102060203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0320307202
- Product Code / EMDN
- W0102060203
- Device Name
- Cortisol Test (FIA)
- Database Sync Date
- 2026-08-09 17:39:34
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 Cortisol Test (FIA)?
The registered manufacturer of record for Cortisol Test (FIA) is Shenzhen Lifotronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for Cortisol Test (FIA)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978139071380.
What classification code is assigned to this device?
This device is registered under product classification code W0102060203.
Similar Classification Devices (W0102060203)
Other Devices by Shenzhen Lifotronic Technology Co., Ltd.
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