25-Hydroxy Vitamin D Test (FIA) (UDI 06978139071335)
Manufactured by Shenzhen Lifotronic Technology Co., Ltd.
Device Regulatory Overview
The 25-Hydroxy Vitamin D Test (FIA) (Model/Catalog Number: 0320305402) is a medical device manufactured by Shenzhen Lifotronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102060309 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0320305402
- Product Code / EMDN
- W0102060309
- Device Name
- 25-Hydroxy Vitamin D Test (FIA)
- Database Sync Date
- 2026-08-09 16:46:41
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 25-Hydroxy Vitamin D Test (FIA)?
The registered manufacturer of record for 25-Hydroxy Vitamin D Test (FIA) is Shenzhen Lifotronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for 25-Hydroxy Vitamin D Test (FIA)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978139071335.
What classification code is assigned to this device?
This device is registered under product classification code W0102060309.
Similar Classification Devices (W0102060309)
Other Devices by Shenzhen Lifotronic Technology Co., Ltd.
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