Taiwan FDA registration b285ed59f06b49e953f6288b9b6bb239
“VACUKANG” Heparin Vacuum Blood Collection Tubes
TW: “永康”肝素真空採血管
Taiwan·Risk Class 2·MD·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Jun 03, 2016 – Jun 03, 2026ExpiredRegistration details
- Analysis ID
- b285ed59f06b49e953f6288b9b6bb239
- License Form
- Ministry of Health Medical Device Manufacturing No. 005178
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
- It is used to collect blood for clinical laboratory testing of plasma or whole blood.
- 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
- Jun 03, 2016
- Expiry Date
- Jun 03, 2026
About this record
Access comprehensive regulatory information for “VACUKANG” Heparin Vacuum 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 b285ed59f06b49e953f6288b9b6bb239 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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