Pure Global

Yijia single-use vacuum blood collection tube (tripotassium ethylenediaminetetraacetate) - Taiwan Registration dfc50272928a61fea19ee235d1ba9014

Access comprehensive regulatory information for Yijia single-use vacuum blood collection tube (tripotassium ethylenediaminetetraacetate) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dfc50272928a61fea19ee235d1ba9014 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
dfc50272928a61fea19ee235d1ba9014
Registration Details
Taiwan FDA Registration: dfc50272928a61fea19ee235d1ba9014
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

dfc50272928a61fea19ee235d1ba9014

DHA04200041404

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

Input;; Chinese goods

Dates and Status

Nov 30, 2011

Nov 30, 2021

Sep 23, 2023

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ