Taiwan FDA registration bd296a35034f54bd373ea7fc16ac7253

"Reed" pregnancy test series

TW: “瑞德” 驗孕測試系列

Taiwan·Risk Class 2·Ruide Biotech Co., Ltd.;; Dongyao Biotechnology Co., Ltd·Registered Oct 18, 2016 – Sep 28, 2025Expired

Registration details

Analysis ID: bd296a35034f54bd373ea7fc16ac7253

Company information

Manufacturer: Ruide Biotech Co., Ltd.;; Dongyao Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: RUI DE BIOTECH CO., LTD.

Product details

Intended Use: The urine is tested qualitatively for human chorionic gonadotropin. New performance: Added non-professional use.
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: Oct 18, 2016
Expiry Date: Sep 28, 2025

About this record

Access comprehensive regulatory information for "Reed" pregnancy test series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd296a35034f54bd373ea7fc16ac7253 and manufactured by Ruide Biotech Co., Ltd.;; Dongyao Biotechnology Co., Ltd. The authorized representative in Taiwan is RUI DE BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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.