Taiwan FDA registration 652c2a5ed2a46fd82669ef578cb5f752
Americanco A+B influenza virus assay
TW: 亞美利可 A+B 型流行性感冒病毒檢驗試劑
Taiwan·Risk Class 1·AMERITEK USA·Registered Sep 02, 2010 – Sep 02, 2020CancelledRegistration details
- Analysis ID
- 652c2a5ed2a46fd82669ef578cb5f752
- Customs Code
- DHA04600104408
Company information
- Manufacturer
- AMERITEK USA
- Manufacturer Country
- China
- Authorized Representative
- LIKWANG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Sep 02, 2010
- Expiry Date
- Sep 02, 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 Americanco A+B influenza virus assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 652c2a5ed2a46fd82669ef578cb5f752 and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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