Taiwan FDA registration e4987c85792947e9f737e4314a80f212
In vitro reagent pen for a Falyer pregnancy test
TW: 法萊兒驗孕體外試劑筆
Taiwan·Risk Class 2·Longteng Biotechnology Co., Ltd·Registered Jan 18, 2012 – Dec 12, 2015CancelledRegistration details
- Analysis ID
- e4987c85792947e9f737e4314a80f212
- Customs Code
- DHY00500351007
Company information
- Manufacturer
- Longteng Biotechnology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YEA CHANCE ENTERPRISE CO., LTD.
Product details
- Intended Use
- Qualitative testing of human pilionic gonadotropins.
- 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
- Jan 18, 2012
- Expiry Date
- Dec 12, 2015
- Cancellation Date
- May 13, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for In vitro reagent pen for a Falyer pregnancy test in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4987c85792947e9f737e4314a80f212 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is YEA CHANCE ENTERPRISE CO., LTD..
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