Taiwan FDA registration 9a7e5d25d25dee05e62396a719e3a7ba
Kim Caisha Rapid Pregnancy Test Pen
TW: 金采帛莎快速驗孕試劑筆
Taiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Jun 30, 2010 – Dec 12, 2020CancelledRegistration details
- Analysis ID
- 9a7e5d25d25dee05e62396a719e3a7ba
- Customs Code
- DHY00500305101
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Xinghai Pharmaceutical Co., Ltd
Product details
- Intended Use
- The concentration of hCG in human urine is measured.
- 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
- Jun 30, 2010
- Expiry Date
- Dec 12, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Kim Caisha Rapid 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 9a7e5d25d25dee05e62396a719e3a7ba and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is Xinghai Pharmaceutical Co., Ltd.
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