Taiwan FDA registration 755bdfbbb4b21ea095597c2e5f83f9dd
Knee ONE Intra-articular Injection
TW: 關益 關節腔注射劑
Taiwan·Risk Class 3·MD·Yongxin Pharmaceutical Industry Co., Ltd. Taichung Lion Factory·Registered May 18, 2023 – May 18, 2028ActiveRegistration details
- Analysis ID
- 755bdfbbb4b21ea095597c2e5f83f9dd
- License Form
- Ministry of Health Medical Device Manufacturing No. 007863
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YUNG SHIN PHARM. IND. CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N0003 Hyaluronic acid implants for the joint cavity
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 18, 2023
- Expiry Date
- May 18, 2028
About this record
Access comprehensive regulatory information for Knee ONE Intra-articular Injection in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 755bdfbbb4b21ea095597c2e5f83f9dd and manufactured by Yongxin Pharmaceutical Industry Co., Ltd. Taichung Lion Factory. The authorized representative in Taiwan is YUNG SHIN PHARM. IND. CO., LTD..
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