Taiwan FDA registration 7b389c06031851e691f95040cebb0429
Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Lithium Heparin Tube)
TW: 麥斯特一次性使用真空採血管(肝素鋰)
Taiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Aug 14, 2014 – Aug 14, 2024ExpiredRegistration details
- Analysis ID
- 7b389c06031851e691f95040cebb0429
- License Form
- Ministry of Health Medical Device Import No. 026504
- Customs Code
- DHA05602650400
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 14, 2014
- Expiry Date
- Aug 14, 2024
About this record
Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Lithium 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 7b389c06031851e691f95040cebb0429 and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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