Taiwan FDA registration 6fd4d092a29ce998838e2fd1e4ad79ef
EasyTouch β-Ketone Control Solution (Non-Sterile)
TW: 易立測 酮體品管液 (未滅菌)
Taiwan·Risk Class 1·MD·BIOPTIK TECHNOLOGY, INC.·Registered Aug 21, 2019 – Aug 21, 2024ExpiredRegistration details
- Analysis ID
- 6fd4d092a29ce998838e2fd1e4ad79ef
- License Form
- Ministry of Health Medical Device Manufacturing No. 007906
Company information
- Manufacturer
- BIOPTIK TECHNOLOGY, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOPTIK TECHNOLOGY, INC.
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
- Aug 21, 2019
- Expiry Date
- Aug 21, 2024
About this record
Access comprehensive regulatory information for EasyTouch β-Ketone 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 6fd4d092a29ce998838e2fd1e4ad79ef and manufactured by BIOPTIK TECHNOLOGY, INC.. The authorized representative in Taiwan is BIOPTIK TECHNOLOGY, INC..
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