Taiwan FDA registration 58c1d8649665e42c275604dc0bc6a8f9
"MagQu" α-Synuclein Control Solution (Non-Sterile)
TW: "磁量" α-突觸核蛋白品管液(未滅菌)
Taiwan·Risk Class 1·MD·MAGQU CO., LTD.·Registered May 16, 2018 – May 16, 2023ExpiredRegistration details
- Analysis ID
- 58c1d8649665e42c275604dc0bc6a8f9
- License Form
- Ministry of Health Medical Device Manufacturing No. 007259
Company information
- Manufacturer
- MAGQU CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MAGQU CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1660 Quality Control Materials (Analytical and Non-Analytical)
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 16, 2018
- Expiry Date
- May 16, 2023
About this record
Access comprehensive regulatory information for "MagQu" α-Synuclein Control Solution (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 58c1d8649665e42c275604dc0bc6a8f9 and manufactured by MAGQU CO., LTD.. The authorized representative in Taiwan is MAGQU CO., LTD..
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