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“Artron” One Step Rapid Diagnostic Test - Ovulation LH Strip Test (Non-Sterile) - Taiwan Registration 7e8ba4d1eea7f81a90e954679def6eaa

Access comprehensive regulatory information for “Artron” One Step Rapid Diagnostic Test - Ovulation LH Strip Test (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 7e8ba4d1eea7f81a90e954679def6eaa and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is WEIYOU TECH INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARTRON LABORATORIES INC., and 1 recent registrations in the same category. 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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7e8ba4d1eea7f81a90e954679def6eaa
Registration Details
Taiwan FDA Registration: 7e8ba4d1eea7f81a90e954679def6eaa
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Device Details

“Artron” One Step Rapid Diagnostic Test - Ovulation LH Strip Test (Non-Sterile)
TW: "愛創" 排卵快速檢測試紙 (未滅菌)
Risk Class 1
MD

Registration Details

7e8ba4d1eea7f81a90e954679def6eaa

Ministry of Health Medical Device Import No. 019517

DHA09401951709

Company Information

Canada

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

Imported from abroad

Dates and Status

Aug 21, 2018

Aug 21, 2023

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