Taiwan FDA registration 4a42c914a7a947e8ede84268d1ddfb69
Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K2 EDTA Tube)
TW: 麥斯特一次性使用真空採血管(乙二胺四乙酸二鉀)
Taiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Apr 30, 2015 – Apr 30, 2025ExpiredRegistration details
- Analysis ID
- 4a42c914a7a947e8ede84268d1ddfb69
- License Form
- Ministry of Health Medical Device Import No. 027326
- Customs Code
- DHA05602732604
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 routine blood [red blood cells, white blood cells, platelets, white blood cell classification, hemoglobin] routine examination.
- 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
- Apr 30, 2015
- Expiry Date
- Apr 30, 2025
About this record
Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K2 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 4a42c914a7a947e8ede84268d1ddfb69 and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..
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