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Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Coagulation Tube) - Taiwan Registration f8b70dfd0fd86f06b6f7586046254512

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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f8b70dfd0fd86f06b6f7586046254512
Registration Details
Taiwan FDA Registration: f8b70dfd0fd86f06b6f7586046254512
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Device Details

Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Coagulation Tube)
TW: ้บฅๆ–ฏ็‰นไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(ๆชธๆชฌ้…ธ้ˆ‰9NC)
Risk Class 2
MD

Registration Details

f8b70dfd0fd86f06b6f7586046254512

Ministry of Health Medical Device Import No. 026505

DHA05602650502

Company Information

Korea, Republic of

Product Details

Blood collection tubes for the detection of blood fiber system.

A Clinical chemistry and clinical toxicology

A1675 Blood Sample Collection Device

Imported from abroad

Dates and Status

Aug 14, 2014

Aug 14, 2024