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Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Sodium Heparin Tube) - Taiwan Registration d50a0e4cd8d33e080c99d38d2584fa8f

Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Sodium Heparin Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d50a0e4cd8d33e080c99d38d2584fa8f and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..

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d50a0e4cd8d33e080c99d38d2584fa8f
Registration Details
Taiwan FDA Registration: d50a0e4cd8d33e080c99d38d2584fa8f
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Device Details

Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Sodium Heparin Tube)
TW: ้บฅๆ–ฏ็‰นไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(่‚็ด ้ˆ‰)
Risk Class 2
MD

Registration Details

d50a0e4cd8d33e080c99d38d2584fa8f

Ministry of Health Medical Device Import No. 027369

DHA05602736909

Company Information

Korea, Republic of

Product Details

Used for emergency biochemistry, plasma biochemical examination of blood collection blood tubes.

A Clinical chemistry and clinical toxicology

A1675 Blood Sample Collection Device

Imported from abroad

Dates and Status

Jul 06, 2015

Jul 06, 2025