Taiwan FDA registration 19de1f3eadfb9bff8cfbad940a0da1c0

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

TW: "亞創" 排卵快速檢測試劑 (未滅菌)

Taiwan·Risk Class 1·MD·ARTRON LABORATORIES INC.·Registered Dec 29, 2015 – Dec 29, 2025Expired

Registration details

Analysis ID: 19de1f3eadfb9bff8cfbad940a0da1c0
License Form: Ministry of Health Medical Device Import No. 016031
Customs Code: DHA09401603107

Company information

Manufacturer: ARTRON LABORATORIES INC.
Manufacturer Country: Canada
Authorized Representative: SUNGYIN BIO INTERNATIONAL 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: Dec 29, 2015
Expiry Date: Dec 29, 2025

About this record

Access comprehensive regulatory information for "Artron" One Step 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 19de1f3eadfb9bff8cfbad940a0da1c0 and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is SUNGYIN BIO INTERNATIONAL CO., LTD..

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