Taiwan FDA registration fc5e2f89b6ee655155631d7636f52a4f

In vitro reagent for Wilden pregnancy test

TW: 威爾登驗孕體外試劑

Taiwan·Risk Class 2·Longteng Biotech Co., Ltd. Xinshi Plant;; Wilden International Trading Co., Ltd·Registered Mar 08, 2019 – Oct 26, 2028Active

Registration details

Analysis ID: fc5e2f89b6ee655155631d7636f52a4f

Company information

Manufacturer: Longteng Biotech Co., Ltd. Xinshi Plant;; Wilden International Trading Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: WELLDENG INTERNATIONAL CO., LTD.

Product details

Intended Use: This product qualitatively detects human chorionic gonadotropins in human urine.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1155 Human chorionic gonadotropin testing system
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Mar 08, 2019
Expiry Date: Oct 26, 2028

About this record

Access comprehensive regulatory information for In vitro reagent for Wilden pregnancy test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc5e2f89b6ee655155631d7636f52a4f and manufactured by Longteng Biotech Co., Ltd. Xinshi Plant;; Wilden International Trading Co., Ltd. The authorized representative in Taiwan is WELLDENG INTERNATIONAL CO., LTD..

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