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Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Serum Plain Tube) - Taiwan Registration 3ba40466ec5efbc962d0d1bbde3f9a7b

Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Serum Plain Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3ba40466ec5efbc962d0d1bbde3f9a7b 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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3ba40466ec5efbc962d0d1bbde3f9a7b
Registration Details
Taiwan FDA Registration: 3ba40466ec5efbc962d0d1bbde3f9a7b
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Device Details

Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Serum Plain Tube)
TW: ้บฅๆ–ฏ็‰นไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(ไฟƒๅ‡ๅŠ‘)
Risk Class 2
MD

Registration Details

3ba40466ec5efbc962d0d1bbde3f9a7b

Ministry of Health Medical Device Import No. 026503

DHA05602650308

Company Information

Korea, Republic of

Product Details

This product is used for blood collection of blood vessels for serum biochemical examination.

A Clinical chemistry and clinical toxicology

A1675 Blood Sample Collection Device

Imported from abroad

Dates and Status

Aug 13, 2014

Aug 13, 2024