Pure Global

Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Serum Separation Gel Tube) - Taiwan Registration 48c450a2ea04773130d44803e251eb66

Access comprehensive regulatory information for Sunmax Single-use Containers for Human Venous Blood Specimen Collection(Serum Separation Gel Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 48c450a2ea04773130d44803e251eb66 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
48c450a2ea04773130d44803e251eb66
Registration Details
Taiwan FDA Registration: 48c450a2ea04773130d44803e251eb66
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

48c450a2ea04773130d44803e251eb66

Ministry of Health Medical Device Import No. 026507

DHA05602650703

Company Information

Korea, Republic of

Product Details

It is used for blood collection blood collection for serum biochemical examination, and centrifugation after blood collection can separate serum and plasma (blood cells).

A Clinical chemistry and clinical toxicology

A1675 Blood Sample Collection Device

Imported from abroad

Dates and Status

Aug 14, 2014

Aug 14, 2024