Taiwan FDA registration 7f169a836b3f9476fbf0d316cb3943c1
Vanokan platelet concentrate tube
TW: 凡諾康血小板濃縮管
Taiwan·Risk Class 2·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered May 31, 2023 – May 31, 2028ActiveRegistration details
- Analysis ID
- 7f169a836b3f9476fbf0d316cb3943c1
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 prepares platelet-rich plasma (PRP) from blood samples.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9245 Automated hemocytoseparator
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- May 31, 2023
- Expiry Date
- May 31, 2028
About this record
Access comprehensive regulatory information for Vanokan platelet concentrate tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f169a836b3f9476fbf0d316cb3943c1 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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