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Eveline Ovulation Test System (Non-Sterile) - Taiwan Registration d7a10ac5adb8c60f4c88a26de427a078

Access comprehensive regulatory information for Eveline Ovulation Test System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d7a10ac5adb8c60f4c88a26de427a078 and manufactured by Inner Lake Plant of AXA Shengke Co., Ltd. The authorized representative in Taiwan is IXENSOR CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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d7a10ac5adb8c60f4c88a26de427a078
Registration Details
Taiwan FDA Registration: d7a10ac5adb8c60f4c88a26de427a078
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Device Details

Eveline Ovulation Test System (Non-Sterile)
TW: ไผŠๅฟ…ๆธฌ ๆŽ’ๅตๆชขๆธฌ็ณป็ตฑ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d7a10ac5adb8c60f4c88a26de427a078

Ministry of Health Medical Device Manufacturing No. 006812

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1485 Progesterone Test System

Produced in Taiwan, China

Dates and Status

Jun 28, 2017

Jun 28, 2027