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Yijia single-use vacuum blood collection blood collection (dipotassium ethylenediaminetetraacetate) - Taiwan Registration 17f25c2b68d32545500174961a281067

Access comprehensive regulatory information for Yijia single-use vacuum blood collection blood collection (dipotassium ethylenediaminetetraacetate) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17f25c2b68d32545500174961a281067 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. 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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17f25c2b68d32545500174961a281067
Registration Details
Taiwan FDA Registration: 17f25c2b68d32545500174961a281067
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Device Details

Yijia single-use vacuum blood collection blood collection (dipotassium ethylenediaminetetraacetate)
TW: ้†ซไฝณไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(ไน™ไบŒ่ƒบๅ››ไน™้…ธไบŒ้‰€)
Risk Class 2
Cancelled

Registration Details

17f25c2b68d32545500174961a281067

DHA04200048705

Company Information

Product Details

It is used for the examination of blood routine [red blood cells, white blood cells, platelets, white blood cell differential, hemoglobin].

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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