Taiwan FDA registration f8b70dfd0fd86f06b6f7586046254512

Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Coagulation Tube)

TW: 麥斯特一次性使用真空採血管(檸檬酸鈉9NC)

Taiwan·Risk Class 2·MD·SOYAGREENTEC CO., LTD·Registered Aug 14, 2014 – Aug 14, 2024Expired

Registration details

Analysis ID: f8b70dfd0fd86f06b6f7586046254512
License Form: Ministry of Health Medical Device Import No. 026505
Customs Code: DHA05602650502

Company information

Manufacturer: SOYAGREENTEC CO., LTD
Manufacturer Country: Korea, Republic of
Authorized Representative: EAFAN ENTERPRISE CO., LTD.

Product details

Intended Use: Blood collection tubes for the detection of blood fiber system.
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(Coagulation Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f8b70dfd0fd86f06b6f7586046254512 and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..

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