Taiwan FDA registration bb9ad576f612ebe827675998c3d00b26
"Yangpu" single-use vacuum blood collection tube (no addition tube)
TW: “陽普”一次性使用真空採血管(無添加管)
Taiwan·Risk Class 2·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.·Registered Sep 16, 2014 – Sep 16, 2029ActiveRegistration details
- Analysis ID
- bb9ad576f612ebe827675998c3d00b26
- Customs Code
- DHA09200062204
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, mainly used for serum clinical chemistry and immunological detection.
- 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 (no addition tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bb9ad576f612ebe827675998c3d00b26 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