Taiwan FDA registration feb007ba51d7328614f0f4ea3ca5d61f
Sunmax Single-use Containers for Human Venous Blood Specimen Collection(ESR Tube)
TW: 麥斯特一次性使用真空採血管(檸檬酸鈉4NC)
Taiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Aug 14, 2014 – Aug 14, 2019CancelledRegistration details
- Analysis ID
- feb007ba51d7328614f0f4ea3ca5d61f
- License Form
- Ministry of Health Medical Device Import No. 026506
- Customs Code
- DHA05602650601
Company information
- Manufacturer
- SOYAGREENTEC CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- AGREE HEALTH CARE TECHNOLOGY, LTD.
Product details
- 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, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(ESR Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number feb007ba51d7328614f0f4ea3ca5d61f and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..
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