eudamed_udi Primary ID: 06975984063256

Testosterone (Electrochemiluminescence Immunoassay) (UDI 06975984063256)

Manufactured by Shenzhen Lifotronic Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Testosterone (Electrochemiluminescence Immunoassay) (Model/Catalog Number: 697036) is a medical device manufactured by Shenzhen Lifotronic Technology 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: 697036
Product Code / EMDN: W0102050110
Device Name: Testosterone (Electrochemiluminescence Immunoassay)
Database Sync Date: 2026-08-09 16:49:13

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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Frequently Asked Questions

Who is the primary manufacturer of Testosterone (Electrochemiluminescence Immunoassay)?

The registered manufacturer of record for Testosterone (Electrochemiluminescence Immunoassay) is Shenzhen Lifotronic Technology Co., Ltd..

What is the Primary UDI-DI identifier for Testosterone (Electrochemiluminescence Immunoassay)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975984063256.

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 Lifotronic Technology Co., Ltd.

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