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Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K3 EDTA Tube) - Taiwan Registration 8177f6b21841c1f4ed5c92678c27f6a9

Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K3 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 8177f6b21841c1f4ed5c92678c27f6a9 and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..

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8177f6b21841c1f4ed5c92678c27f6a9
Registration Details
Taiwan FDA Registration: 8177f6b21841c1f4ed5c92678c27f6a9
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Device Details

Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K3 EDTA Tube)
TW: ้บฅๆ–ฏ็‰นไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(ไน™ไบŒ่ƒบๅ››ไน™้…ธไธ‰้‰€)
Risk Class 2
MD

Registration Details

8177f6b21841c1f4ed5c92678c27f6a9

Ministry of Health Medical Device Import No. 026300

DHA05602630007

Company Information

Korea, Republic of

Product Details

This product is used for blood routine [red blood cells, white blood cells, platelets, white blood cell classification, hemoglobin] detection of blood collection blood tubes.

A Clinical chemistry and clinical toxicology

A1675 Blood Sample Collection Device

Imported from abroad

Dates and Status

Aug 13, 2014

Aug 13, 2024