Taiwan FDA registration bf6eeb4d62f12613e6fe829cc6d9522a
Kim Cai Shu Sha Rapid Pregnancy Test Card
TW: 金采帛莎快速驗孕試劑卡
Taiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Jun 30, 2010 – Feb 09, 2021CancelledRegistration details
- Analysis ID
- bf6eeb4d62f12613e6fe829cc6d9522a
- Customs Code
- DHY00500305002
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Xinghai Pharmaceutical Co., Ltd
Product details
- Intended Use
- It is used as a test reagent for early diagnosis of pregnancy
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Jun 30, 2010
- Expiry Date
- Feb 09, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Kim Cai Shu Sha Rapid Pregnancy Test Card in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf6eeb4d62f12613e6fe829cc6d9522a 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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