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“Artron” One Step Rapid Diagnostic Test - Ovulation LH Strip Test (Non-Sterile) - Taiwan Registration 1cbdd7e03e739a3adc1cc527d70ce72a

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 1cbdd7e03e739a3adc1cc527d70ce72a and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is GORED ENTERPRISE CO., LTD..

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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1cbdd7e03e739a3adc1cc527d70ce72a
Registration Details
Taiwan FDA Registration: 1cbdd7e03e739a3adc1cc527d70ce72a
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Device Details

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

Registration Details

1cbdd7e03e739a3adc1cc527d70ce72a

Ministry of Health Medical Device Import No. 014759

DHA09401475908

Company Information

Canada

Product Details

Limited to the first level identification range of the "luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Equipment.

A Clinical chemistry and clinical toxicology

A1485 Luteinizing Gonadotropin Test System

Imported from abroad

Dates and Status

Dec 17, 2014

Dec 17, 2024

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