Taiwan FDA registration aa88873f12721ad38608a5835260ce67
"Yangpu" single-use vacuum blood collection tube (procoagulant tube)
TW: “陽普”一次性使用真空採血管(促凝管)
Taiwan·Risk Class 2·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.·Registered Sep 16, 2014 – Sep 16, 2029ActiveRegistration details
- Analysis ID
- aa88873f12721ad38608a5835260ce67
- Customs Code
- DHA09200062306
Company information
- Manufacturer
- GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BEAM INTERNATIONAL INC.
Product details
- Intended Use
- This product is a vacuum container for the collection, storage, transportation and processing of venous blood samples, which can be used for serum clinical chemistry and immunological testing.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1675 Blood collection equipment
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Sep 16, 2014
- Expiry Date
- Sep 16, 2029
About this record
Access comprehensive regulatory information for "Yangpu" single-use vacuum blood collection tube (procoagulant tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa88873f12721ad38608a5835260ce67 and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..
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