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Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K2 EDTA Tube) - Taiwan Registration 4a42c914a7a947e8ede84268d1ddfb69

Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K2 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 4a42c914a7a947e8ede84268d1ddfb69 and manufactured by SOYAGREENTEC CO., LTD. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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4a42c914a7a947e8ede84268d1ddfb69
Registration Details
Taiwan FDA Registration: 4a42c914a7a947e8ede84268d1ddfb69
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Device Details

Sunmax Single-use Containers for Human Venous Blood Specimen Collection(K2 EDTA Tube)
TW: ้บฅๆ–ฏ็‰นไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(ไน™ไบŒ่ƒบๅ››ไน™้…ธไบŒ้‰€)
Risk Class 2
MD

Registration Details

4a42c914a7a947e8ede84268d1ddfb69

Ministry of Health Medical Device Import No. 027326

DHA05602732604

Company Information

Korea, Republic of

Product Details

This product is used for routine blood [red blood cells, white blood cells, platelets, white blood cell classification, hemoglobin] routine examination.

A Clinical chemistry and clinical toxicology

A1675 Blood Sample Collection Device

Imported from abroad

Dates and Status

Apr 30, 2015

Apr 30, 2025