Taiwan FDA registration d50a0e4cd8d33e080c99d38d2584fa8f
Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Sodium Heparin Tube)
TW: 麥斯特一次性使用真空採血管(肝素鈉)
Taiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Jul 06, 2015 – Jul 06, 2025ExpiredRegistration details
- Analysis ID
- d50a0e4cd8d33e080c99d38d2584fa8f
- License Form
- Ministry of Health Medical Device Import No. 027369
- Customs Code
- DHA05602736909
Company information
- Manufacturer
- SOYAGREENTEC CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EAFAN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Used for emergency biochemistry, plasma biochemical examination of blood collection blood 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
- Jul 06, 2015
- Expiry Date
- Jul 06, 2025
About this record
Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(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 d50a0e4cd8d33e080c99d38d2584fa8f and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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