Testosterone (T) Diagnostic Kit (UDI 06971348760304)
Manufactured by Shenzhen Microprofit Biotech Co., Ltd
Device Regulatory Overview
The Testosterone (T) Diagnostic Kit (Model/Catalog Number: MF-18-20) is a medical device manufactured by Shenzhen Microprofit Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102050110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MF-18-20
- Product Code / EMDN
- W0102050110
- Device Name
- Testosterone (T) Diagnostic Kit
- 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 Testosterone (T) Diagnostic Kit?
The registered manufacturer of record for Testosterone (T) Diagnostic Kit is Shenzhen Microprofit Biotech Co., Ltd.
What is the Primary UDI-DI identifier for Testosterone (T) Diagnostic Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971348760304.
What classification code is assigned to this device?
This device is registered under product classification code W0102050110.
Similar Classification Devices (W0102050110)
Other Devices by Shenzhen Microprofit Biotech Co., Ltd
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