Taiwan FDA registration 67499cf8be93625baf5b68eafffee908
"Yongkang" EDTAX vacuum blood collection vessels
TW: “永康” 乙二胺四乙酸二鉀真空採血管
Taiwan·Risk Class 2·YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.·Registered Aug 19, 2011 – Aug 19, 2026ActiveRegistration details
- Analysis ID
- 67499cf8be93625baf5b68eafffee908
- Customs Code
- DHY00500339701
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)
- A.1675 Blood collection equipment
- Import Information
- Domestic
Dates and status
- Registration Date
- Aug 19, 2011
- Expiry Date
- Aug 19, 2026
About this record
Access comprehensive regulatory information for "Yongkang" EDTAX vacuum blood collection vessels in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67499cf8be93625baf5b68eafffee908 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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