Taiwan FDA registration 0fc832c8ec91e9203f1c00c196b083ff
New human pregnancy test reagent series
TW: 新人類驗孕試劑系列
Taiwan·Risk Class 2·The first factory of Longteng Biotechnology Co., Ltd·Registered Jan 04, 2008 – Dec 12, 2020CancelledRegistration details
- Analysis ID
- 0fc832c8ec91e9203f1c00c196b083ff
- Customs Code
- DHY00500257504
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHANQ-YU DRUG TRADING 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
- Domestic
Dates and status
- Registration Date
- Jan 04, 2008
- 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 New human pregnancy test reagent series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0fc832c8ec91e9203f1c00c196b083ff and manufactured by The first factory of Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is SHANQ-YU DRUG TRADING CO., LTD..
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