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Yijia single-use vacuum blood collection tube (lithium heparin) - Taiwan Registration c43247433e7529a8188bda50e6096c4a

Access comprehensive regulatory information for Yijia single-use vacuum blood collection tube (lithium heparin) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c43247433e7529a8188bda50e6096c4a 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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c43247433e7529a8188bda50e6096c4a
Registration Details
Taiwan FDA Registration: c43247433e7529a8188bda50e6096c4a
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Device Details

Yijia single-use vacuum blood collection tube (lithium heparin)
TW: ้†ซไฝณไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(่‚็ด ้‹ฐ)
Risk Class 2
Cancelled

Registration Details

c43247433e7529a8188bda50e6096c4a

DHA04200041101

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

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