Taiwan FDA registration f09850e37bc5db770463aae6dc7e6472

Quick and easy test of in vitro progesto

TW: 快易測驗孕體外試劑

Taiwan·Risk Class 2·Longteng Biotechnology Co., Ltd. Xinshi Factory;; Liyang Biotechnology Co., Ltd·Registered Nov 22, 2019 – Oct 26, 2023Expired

Registration details

Analysis ID: f09850e37bc5db770463aae6dc7e6472

Company information

Manufacturer: Longteng Biotechnology Co., Ltd. Xinshi Factory;; Liyang Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BIOLINK SCIENTIFIC INC.

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: Nov 22, 2019
Expiry Date: Oct 26, 2023

About this record

Access comprehensive regulatory information for Quick and easy test of in vitro progesto in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f09850e37bc5db770463aae6dc7e6472 and manufactured by Longteng Biotechnology Co., Ltd. Xinshi Factory;; Liyang Biotechnology Co., Ltd. The authorized representative in Taiwan is BIOLINK SCIENTIFIC INC..

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