Taiwan FDA registration 3bd4dc58dbfb4fcdfc67adec3933959f

Artron Human Chorionic Gonadotropin (HCG) Test System

TW: 雅創驗孕測試系列

Taiwan·Risk Class 2·MD·ARTRON LABORATORIES INC.·Registered Sep 05, 2018 – Sep 05, 2023Expired

Registration details

Analysis ID: 3bd4dc58dbfb4fcdfc67adec3933959f
License Form: Ministry of Health Medical Device Import No. 031454
Customs Code: DHA05603145402

Company information

Manufacturer: ARTRON LABORATORIES INC.
Manufacturer Country: Canada
Authorized Representative: GORED ENTERPRISE CO., LTD.

Product details

Intended Use: Human chorionic gonadotropin (HCG) in urine was tested by immunoqualitative analysis and preliminarily screened for pregnancy. Available for professional and non-professional use.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1155 Human chorionic gonadotropin test system
Import Information: Imported from abroad

Dates and status

Registration Date: Sep 05, 2018
Expiry Date: Sep 05, 2023

About this record

Access comprehensive regulatory information for Artron Human Chorionic Gonadotropin (HCG) Test System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3bd4dc58dbfb4fcdfc67adec3933959f and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is GORED ENTERPRISE CO., LTD..

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