Taiwan FDA registration 8177f6b21841c1f4ed5c92678c27f6a9
Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K3 EDTA Tube)
TW: 麥斯特一次性使用真空採血管(乙二胺四乙酸三鉀)
Taiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Aug 13, 2014 – Aug 13, 2024ExpiredRegistration details
- Analysis ID
- 8177f6b21841c1f4ed5c92678c27f6a9
- License Form
- Ministry of Health Medical Device Import No. 026300
- Customs Code
- DHA05602630007
Company information
- Manufacturer
- SOYAGREENTEC CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EAFAN ENTERPRISE CO., LTD.
Product details
- Intended Use
- This product is used for blood routine [red blood cells, white blood cells, platelets, white blood cell classification, hemoglobin] detection 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
- 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(K3 EDTA Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8177f6b21841c1f4ed5c92678c27f6a9 and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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