Taiwan FDA registration 0cbb78b0c304e88df4be5698b7f9328d
Medical single-use vacuum blood collection tube (tripotassium ethylenediaminetetraacetate)
TW: 醫凡一次性使用真空採血管(乙二胺四乙酸三鉀)
Taiwan·Risk Class 2·HEBEI XINLE SCI & TECH CO., LTD.·Registered Dec 20, 2018 – Dec 20, 2028ActiveRegistration details
- Analysis ID
- 0cbb78b0c304e88df4be5698b7f9328d
- Customs Code
- DHA09200099201
Company information
- Manufacturer
- HEBEI XINLE SCI & TECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- EAFAN ENTERPRISE CO., LTD.
Product details
- Intended Use
- This product is used for routine blood (red blood cells, white blood cells, platelets, white blood cell classification, hemoglobin).
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1675 Blood collection equipment
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Dec 20, 2018
- Expiry Date
- Dec 20, 2028
About this record
Access comprehensive regulatory information for Medical single-use vacuum blood collection tube (tripotassium ethylenediaminetetraacetate) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0cbb78b0c304e88df4be5698b7f9328d and manufactured by HEBEI XINLE SCI & TECH CO., LTD.. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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