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Yijia single-use vacuum blood collection (heparin sodium) - Taiwan Registration 752741d0f2b4b8d3f9905c144cd9cf43

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 752741d0f2b4b8d3f9905c144cd9cf43 and manufactured by HEBEI XINLE SCI&TECH CO., LTD.. The authorized representative in Taiwan is AGREE HEALTH CARE TECHNOLOGY, LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUZHOU CHANGGENG MEDICAL DEVICES 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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752741d0f2b4b8d3f9905c144cd9cf43
Registration Details
Taiwan FDA Registration: 752741d0f2b4b8d3f9905c144cd9cf43
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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

752741d0f2b4b8d3f9905c144cd9cf43

DHA09200061902

Company Information

Product Details

It is used for emergency biochemical and plasma biochemical examination of blood collection tubes.

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

Input;; Chinese goods

Dates and Status

Aug 05, 2014

Aug 05, 2019

Aug 05, 2022

Cancellation Information

Logged out

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