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Yijia single-use vacuum blood collection (heparin sodium) - Taiwan Registration 492a3902aaf0cdc2db471014a928c08d

Access comprehensive regulatory information for Yijia single-use vacuum blood collection (heparin sodium) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 492a3902aaf0cdc2db471014a928c08d and manufactured by FUZHOU CHANGGENG MEDICAL DEVICES CO., LTD. The authorized representative in Taiwan is Sunray Health Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HEBEI XINLE SCI&TECH CO., LTD., and 1 recent registrations in the same category. 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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492a3902aaf0cdc2db471014a928c08d
Registration Details
Taiwan FDA Registration: 492a3902aaf0cdc2db471014a928c08d
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Device Details

Yijia single-use vacuum blood collection (heparin sodium)
TW: ้†ซไฝณไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(่‚็ด ้ˆ‰)
Risk Class 2
Cancelled

Registration Details

492a3902aaf0cdc2db471014a928c08d

DHA04200048603

Company Information

Product Details

It is used for emergency biochemical and plasma biochemical examination.

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

Input;; Chinese goods

Dates and Status

Feb 21, 2013

Feb 21, 2018

Dec 20, 2019

Cancellation Information

Logged out

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