Taiwan FDA registration a381b3d22a1df1d61f7694d2f590c1fc
Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Lithium Heparin with Gel Tube)
TW: 麥斯特一次性使用真空採血管(肝素鋰/分離膠)
Taiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Aug 13, 2014 – Aug 13, 2024ExpiredRegistration details
- Analysis ID
- a381b3d22a1df1d61f7694d2f590c1fc
- License Form
- Ministry of Health Medical Device Import No. 026501
- Customs Code
- DHA05602650104
Company information
- Manufacturer
- SOYAGREENTEC CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EAFAN ENTERPRISE CO., LTD.
Product details
- Intended Use
- It is used for emergency biochemical and plasma biochemical examination of blood collection tubes.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1675 Blood Sample Collection Device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 13, 2014
- Expiry Date
- Aug 13, 2024
About this record
Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Lithium Heparin with Gel Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a381b3d22a1df1d61f7694d2f590c1fc and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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