Taiwan FDA registration 9283954ed17597ba461617b145184d8d
"VACUKANG" Clot Activator Blood Collection Tubes
TW: “永康”促凝劑真空採血管
Taiwan·Risk Class 2·MD·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Sep 18, 2013 – Sep 18, 2028ActiveRegistration details
- Analysis ID
- 9283954ed17597ba461617b145184d8d
- License Form
- Ministry of Health Medical Device Manufacturing No. 004166
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
- Used to collect blood for serotesting in clinical laboratories.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1675 Blood Sample Collection Device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 18, 2013
- Expiry Date
- Sep 18, 2028
About this record
Access comprehensive regulatory information for "VACUKANG" Clot Activator Blood Collection Tubes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9283954ed17597ba461617b145184d8d 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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