Taiwan FDA registration dc1b11f8dd7815335dc3f065d8154f07
“Improvacuter” Evacuated Blood Collection Tube (Sodium Heparin Tube)
TW: “陽普” 一次性使用真空採血管(肝素鈉管)
Taiwan·Risk Class 2·MD·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.·Registered Sep 25, 2014 – Sep 25, 2024ExpiredRegistration details
- Analysis ID
- dc1b11f8dd7815335dc3f065d8154f07
- License Form
- Ministry of Health Medical Device Land Transport No. 000625
- Customs Code
- DHA09200062500
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 plasma biochemical testing in clinical laboratories, and is not suitable for sodium determination.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1675 Blood Sample Collection Device
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Sep 25, 2014
- Expiry Date
- Sep 25, 2024
About this record
Access comprehensive regulatory information for “Improvacuter” Evacuated Blood Collection Tube (Sodium Heparin Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc1b11f8dd7815335dc3f065d8154f07 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