Taiwan FDA registration 2d302e4f836d6cec2dc541e972c6f861
"Rest" titanium sternum fixation system
TW: “芮思特”鈦金屬胸骨固定系統
Taiwan·Risk Class 2·BAUI BIOTECH CO., LTD.·Registered Aug 07, 2023 – Aug 07, 2028ActiveRegistration details
- Analysis ID
- 2d302e4f836d6cec2dc541e972c6f861
Company information
- Manufacturer
- BAUI BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Foresee Medical Ltd.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3030 Single or multiple metallic bone fixation devices and accessories
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Aug 07, 2023
- Expiry Date
- Aug 07, 2028
About this record
Access comprehensive regulatory information for "Rest" titanium sternum fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2d302e4f836d6cec2dc541e972c6f861 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is Foresee Medical Ltd..
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