Taiwan FDA registration e01db0129bd9ac7b0b269434542dbf09
"Yongkang" sodium citrate vacuum blood collection blood vessels
TW: “永康”檸檬酸鈉真空採血管
Taiwan·Risk Class 2·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Jun 13, 2013 – Jun 13, 2028ActiveRegistration details
- Analysis ID
- e01db0129bd9ac7b0b269434542dbf09
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 clinical laboratory testing of plasma or whole blood, suitable for routine coagulation tests.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1675 Blood collection equipment
- Import Information
- Domestic
Dates and status
- Registration Date
- Jun 13, 2013
- Expiry Date
- Jun 13, 2028
About this record
Access comprehensive regulatory information for "Yongkang" sodium citrate vacuum blood collection blood vessels in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e01db0129bd9ac7b0b269434542dbf09 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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