Taiwan FDA registration 621c8ea721929f313aec959cf4b95327
"Core Generation" Mycobacterium tuberculosis immune reagent (unsterilized)
TW: "芯世代" 結核桿菌免疫試劑 (未滅菌)
Taiwan·Risk Class 1·Xintang Enterprise Co., Ltd. Taichung Factory·Registered Oct 24, 2016 – Oct 24, 2021CancelledRegistration details
- Analysis ID
- 621c8ea721929f313aec959cf4b95327
Company information
- Manufacturer
- Xintang Enterprise Co., Ltd. Taichung Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENPRONEX INC.
Product details
- Intended Use
- Limited to the first level identification range of Mycobacterium tuberculosis immunofluorescent reagent (C.3370) of the management method for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3370 結核桿菌免疫螢光試劑
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Oct 24, 2016
- Expiry Date
- Oct 24, 2021
- Cancellation Date
- Apr 20, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Core Generation" Mycobacterium tuberculosis immune 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 621c8ea721929f313aec959cf4b95327 and manufactured by Xintang Enterprise Co., Ltd. Taichung Factory. The authorized representative in Taiwan is GENPRONEX INC..
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