Testosterone Kit (CLIA) (UDI 06936595751468)
Manufactured by MedicalSystem Biotechnology Co., Ltd.
Device Regulatory Overview
The Testosterone Kit (CLIA) (Model/Catalog Number: FG1304Y) is a medical device manufactured by MedicalSystem Biotechnology 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
- FG1304Y
- Product Code / EMDN
- W0102050110
- Device Name
- Testosterone Kit (CLIA)
- Database Sync Date
- 2026-08-09 16:59:51
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 Kit (CLIA)?
The registered manufacturer of record for Testosterone Kit (CLIA) is MedicalSystem Biotechnology Co., Ltd..
What is the Primary UDI-DI identifier for Testosterone Kit (CLIA)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936595751468.
What classification code is assigned to this device?
This device is registered under product classification code W0102050110.
Similar Classification Devices (W0102050110)
Other Devices by MedicalSystem Biotechnology Co., Ltd.
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