Taiwan FDA registration 7e8ba4d1eea7f81a90e954679def6eaa

“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)
Taiwan flagTaiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Aug 21, 2018 – Aug 21, 2023Expired
Registration details
Analysis ID
7e8ba4d1eea7f81a90e954679def6eaa
License Form
Ministry of Health Medical Device Import No. 019517
Customs Code
DHA09401951709
Company information
Manufacturer Country
Canada
Authorized Representative
WEIYOU TECH INC.
Product details
Intended Use
Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1485 Progesterone Test System
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 21, 2018
Expiry Date
Aug 21, 2023
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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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