Taiwan FDA registration f280271c09f51f40452169e6e2ac833e
"Americo" Clostridium difficile toxin A/B screening reagent (unsterilized)
TW: "亞美利可"困難梭狀芽胞桿菌毒素A/B篩檢試劑(未滅菌)
Taiwan·Risk Class 1·AMERITEK USA·Registered Aug 27, 2015 – Aug 27, 2020CancelledRegistration details
- Analysis ID
- f280271c09f51f40452169e6e2ac833e
- Customs Code
- DHA09600248204
Company information
- Manufacturer
- AMERITEK USA
- Manufacturer Country
- China
- Authorized Representative
- LIKWANG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2660 微生物鑑別及測定器材
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 27, 2015
- Expiry Date
- Aug 27, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Americo" Clostridium difficile toxin A/B screening 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 f280271c09f51f40452169e6e2ac833e and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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