Taiwan FDA registration e132ab9f81e6e93d746181579a7e78af
Americo Helicobacter pylori test (unsterilized)
TW: 亞美利可幽門螺旋桿菌檢驗試劑(未滅菌)
Taiwan·Risk Class 1·AMERITEK USA·Registered Jul 16, 2010 – Jul 16, 2020CancelledRegistration details
- Analysis ID
- e132ab9f81e6e93d746181579a7e78af
- Customs Code
- DHA04600097600
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 "Helicobacter Serological Reagent (C.0003)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0003 螺旋桿菌屬血清試劑
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Jul 16, 2010
- Expiry Date
- Jul 16, 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 Helicobacter pylori test (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e132ab9f81e6e93d746181579a7e78af and manufactured by AMERITEK USA. The authorized representative in Taiwan is LIKWANG INSTRUMENTS CO., LTD..
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