Taiwan FDA registration 286f62691a3820adf9e43e60983e9c6e
"Americo" type A streptococcal reagent (unsterilized)
TW: "亞美利可" A型鏈球菌試劑 (未滅菌)
Taiwan·Risk Class 1·AMERITEK USA·Registered Aug 30, 2011 – Aug 30, 2021CancelledRegistration details
- Analysis ID
- 286f62691a3820adf9e43e60983e9c6e
- Customs Code
- DHA04600145302
Company information
- Manufacturer
- AMERITEK USA
- Manufacturer Country
- China
- Authorized Representative
- LIKWANG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3740 鏈球菌屬血清試劑
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 30, 2011
- Expiry Date
- Aug 30, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Americo" type A streptococcal 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 286f62691a3820adf9e43e60983e9c6e and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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