Taiwan FDA registration d6051d96b2926a0826525a92483b13b5
"Taifu" Sulidine Mycoplasma testing reagent (unsterilized)
TW: "台富"速樂定 黴漿菌檢驗試劑(未滅菌)
Taiwan·Risk Class 1·Taiwan Fu Pharmaceutical Co., Ltd·Registered Sep 27, 2005 – Sep 27, 2025CancelledRegistration details
- Analysis ID
- d6051d96b2926a0826525a92483b13b5
- Customs Code
- DHY04300026002
Company information
- Manufacturer
- Taiwan Fu Pharmaceutical Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Taiwan Fu Pharmaceutical Co., Ltd
Product details
- Intended Use
- 檢測血清或血漿中之Mycoplasma抗體力價.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3375 黴漿菌屬血清試劑
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 27, 2005
- Expiry Date
- Sep 27, 2025
- Cancellation Date
- Oct 28, 2022
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Taifu" Sulidine Mycoplasma testing reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d6051d96b2926a0826525a92483b13b5 and manufactured by Taiwan Fu Pharmaceutical Co., Ltd. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.
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