Taiwan FDA registration c1191096affdf3d7f4e44f0dc9dc9c81
Longteng pregnancy test in vitro reagent card
TW: 龍騰驗孕體外試劑卡
Taiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Feb 09, 2006 – Feb 09, 2021CancelledRegistration details
- Analysis ID
- c1191096affdf3d7f4e44f0dc9dc9c81
- Customs Code
- DHY00500198008
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- The first factory of Longteng Biotechnology 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
Dates and status
- Registration Date
- Feb 09, 2006
- Expiry Date
- Feb 09, 2021
- Cancellation Date
- Sep 08, 2022
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for Longteng pregnancy test in vitro reagent card in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c1191096affdf3d7f4e44f0dc9dc9c81 and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is The first factory of Longteng Biotechnology Co., Ltd.
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