Taiwan FDA registration 02171f4ab94d66c0c103164229ba1da5
OYE Rapid Pregnancy Test Series
TW: 歐業快速驗孕測試系列
Taiwan·Risk Class 2·Ouye Pharmaceutical Co., Ltd.; Dongyao Biotechnology Co., Ltd·Registered Sep 30, 2017 – Sep 28, 2025ExpiredRegistration details
- Analysis ID
- 02171f4ab94d66c0c103164229ba1da5
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- OU-YEH PHARMACEUTICAL CO., LTD.
Product details
- Intended Use
- The urine is tested for whether it contains human chorionic gonadotropin (HCG).
- 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
- Sep 30, 2017
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for OYE Rapid 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 02171f4ab94d66c0c103164229ba1da5 and manufactured by Ouye Pharmaceutical Co., Ltd.; Dongyao Biotechnology Co., Ltd. The authorized representative in Taiwan is OU-YEH PHARMACEUTICAL CO., LTD..
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