Taiwan FDA registration e5d29f04361df538178407d0ae1336c4
The new second generation of the pregnancy test series
TW: 快適得驗孕試劑系列新二代
Taiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Feb 05, 2009 – Dec 12, 2020CancelledRegistration details
- Analysis ID
- e5d29f04361df538178407d0ae1336c4
- Customs Code
- DHY00500272306
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KING WARE ENTERPRISE CORP.
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
- Domestic
Dates and status
- Registration Date
- Feb 05, 2009
- Expiry Date
- Dec 12, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for The new second generation of the 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 e5d29f04361df538178407d0ae1336c4 and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is KING WARE ENTERPRISE CORP..
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