Taiwan FDA registration 5c55234914da45c09c7b402123cd727e
"VACUKANG" Clot Activator + Gel Blood Collection Tubes
TW: “永康”促凝劑+分離膠真空採血管
Taiwan·Risk Class 2·MD·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Oct 16, 2013 – Oct 16, 2028ActiveRegistration details
- Analysis ID
- 5c55234914da45c09c7b402123cd727e
- License Form
- Ministry of Health Medical Device Manufacturing No. 004171
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
- Change in efficacy (change in narrative): 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
- Oct 16, 2013
- Expiry Date
- Oct 16, 2028
About this record
Access comprehensive regulatory information for "VACUKANG" Clot Activator + Gel 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 5c55234914da45c09c7b402123cd727e 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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