Taiwan FDA registration 551bf4597264c93c7fb8d9f1356c6837
"Yangpu" single-use vacuum blood collection tubes (blood routine tubes)
TW: “陽普” 一次性使用真空採血管(血常規管)
Taiwan·Risk Class 2·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.·Registered Oct 08, 2014 – Oct 08, 2029ActiveRegistration details
- Analysis ID
- 551bf4597264c93c7fb8d9f1356c6837
- Customs Code
- DHA09200062905
Company information
- Manufacturer
- GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- BEAM INTERNATIONAL INC.
Product details
- Intended Use
- It is used to collect blood for routine testing of whole blood in clinical laboratories.
- 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
- Oct 08, 2014
- Expiry Date
- Oct 08, 2029
About this record
Access comprehensive regulatory information for "Yangpu" single-use vacuum blood collection tubes (blood routine tubes) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 551bf4597264c93c7fb8d9f1356c6837 and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..
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