Taiwan FDA registration 76c97376e4a973fcc3e33a5e0769e52d
"Quick test" Shigella rapid test reagent (unsterilized)
TW: “速測”志賀桿菌快速檢驗試劑(未滅菌)
Taiwan·Risk Class 1·CERTEST BIOTEC S.L.·Registered Apr 06, 2012 – Apr 06, 2017CancelledRegistration details
- Analysis ID
- 76c97376e4a973fcc3e33a5e0769e52d
- Customs Code
- DHA04401156806
Company information
- Manufacturer
- CERTEST BIOTEC S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- JOLEX INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of Shigella serological reagents (C.3660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3660 志賀氏桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Apr 06, 2012
- Expiry Date
- Apr 06, 2017
- Cancellation Date
- Jan 17, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Quick test" Shigella rapid test 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 76c97376e4a973fcc3e33a5e0769e52d and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..
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