Taiwan FDA registration ae39fefe6d01392ada1a2243c3ac234a
"Rest" funnel chest correction system
TW: “芮思特”漏斗胸矯正系統
Taiwan·Risk Class 2·BAUI BIOTECH CO., LTD.·Registered Nov 23, 2022 – Nov 23, 2027ActiveRegistration details
- Analysis ID
- ae39fefe6d01392ada1a2243c3ac234a
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
- Nov 23, 2022
- Expiry Date
- Nov 23, 2027
About this record
Access comprehensive regulatory information for "Rest" funnel chest correction system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae39fefe6d01392ada1a2243c3ac234a and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is Foresee Medical Ltd..
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