Taiwan FDA registration 116ad81919516210b09394eafecaa473
FilmArray RP Control Panel M210 v1.1 (Non-Sterile)
TW: 微晶 呼吸道品管試劑套組 (未滅菌)
Taiwan·Risk Class 1·MD·Maine Molecular Quality Controls, Inc.·Registered Jul 03, 2017 – Jul 03, 2022ExpiredRegistration details
- Analysis ID
- 116ad81919516210b09394eafecaa473
- License Form
- Ministry of Health Medical Device Import No. 018032
- Customs Code
- DHA09401803206
Company information
- Manufacturer
- Maine Molecular Quality Controls, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEGA BONA INTERNATIONAL 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
- Imported from abroad
Dates and status
- Registration Date
- Jul 03, 2017
- Expiry Date
- Jul 03, 2022
About this record
Access comprehensive regulatory information for FilmArray RP Control Panel M210 v1.1 (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 116ad81919516210b09394eafecaa473 and manufactured by Maine Molecular Quality Controls, Inc.. The authorized representative in Taiwan is MEGA BONA INTERNATIONAL CO., LTD..
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