Taiwan FDA registration e47a2dfc5ecf50bc65c04df17e4f4f11
“YK” Platelet-Rich Plasma Concentrate Kit
TW: “永康”血小板濃縮器
Taiwan·Risk Class 2·MD·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Aug 09, 2017 – Aug 09, 2027ActiveRegistration details
- Analysis ID
- e47a2dfc5ecf50bc65c04df17e4f4f11
- License Form
- Ministry of Health Medical Device Manufacturing No. 005633
Company information
- Manufacturer
- YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.
Product details
- Intended Use
- This product can be isolated from blood samples to prepare platelet-rich plasma (PRP). When clinically indicated, platelet thick fluid can be used for mixed autologous and allogeneic orthopedic surgery.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B9245 Automatic Hematology Cell Separator
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 09, 2017
- Expiry Date
- Aug 09, 2027
About this record
Access comprehensive regulatory information for “YK” Platelet-Rich Plasma Concentrate Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e47a2dfc5ecf50bc65c04df17e4f4f11 and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD..
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