Taiwan FDA registration 1ad5cda2534d3a26f9bb146c3e81ec6b
"Yangpu" single-use vacuum blood collection tube (sodium citrate 9:1 tube)
TW: "陽普"一次性使用真空採血管(檸檬酸鈉9:1管)
Registration details
- Analysis ID
- 1ad5cda2534d3a26f9bb146c3e81ec6b
- Customs Code
- DHA09200062602
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 plasma coagulation tests 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 02, 2014
- Expiry Date
- Oct 02, 2029
About this record
Access comprehensive regulatory information for "Yangpu" single-use vacuum blood collection tube (sodium citrate 9:1 tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ad5cda2534d3a26f9bb146c3e81ec6b and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices