Taiwan FDA registration 48c450a2ea04773130d44803e251eb66
Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Serum Separation Gel Tube)
TW: 麥斯特一次性使用真空採血管 (分離膠/促凝劑)
Taiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Aug 14, 2014 – Aug 14, 2024ExpiredRegistration details
- Analysis ID
- 48c450a2ea04773130d44803e251eb66
- License Form
- Ministry of Health Medical Device Import No. 026507
- Customs Code
- DHA05602650703
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 blood collection blood collection for serum biochemical examination, and centrifugation after blood collection can separate serum and plasma (blood cells).
- 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(Serum Separation 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 48c450a2ea04773130d44803e251eb66 and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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