Taiwan FDA registration 9d8728241cf2f37addb9e8b265628811

"Artron" One Step Urine LH Ovulation Test (Non-Sterile)

TW: "恩創" 快速排卵檢測試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Mar 28, 2017 – Mar 28, 2022Expired
Registration details
Analysis ID
9d8728241cf2f37addb9e8b265628811
License Form
Ministry of Health Medical Device Import No. 017652
Customs Code
DHA09401765205
Company information
Manufacturer Country
Canada
Authorized Representative
WELL NOVA CO., LTD.
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
Mar 28, 2017
Expiry Date
Mar 28, 2022
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About this record

Access comprehensive regulatory information for "Artron" One Step Urine LH Ovulation 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 9d8728241cf2f37addb9e8b265628811 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is WELL NOVA 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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