Taiwan FDA registration f30e8a56dc2c080b36d3288401bf8db6
Fore Simple Pregnancy Test Pen
TW: 福爾簡易式驗孕筆
Taiwan·Risk Class 2·Taibo Technology Co., Ltd. five-stock factory·Registered Jan 18, 2012 – Jan 18, 2027ActiveRegistration details
- Analysis ID
- f30e8a56dc2c080b36d3288401bf8db6
- Customs Code
- DHY00500350705
Company information
- Manufacturer
- Taibo Technology Co., Ltd. five-stock factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIDOC TECHNOLOGY CORPORATION
Product details
- Intended Use
- This product qualitatively detects human chorionic gonadotropin (hCG) in urine through a specific reaction between antigens and antibodies.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 18, 2012
- Expiry Date
- Jan 18, 2027
About this record
Access comprehensive regulatory information for Fore Simple Pregnancy Test Pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f30e8a56dc2c080b36d3288401bf8db6 and manufactured by Taibo Technology Co., Ltd. five-stock factory. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.
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