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"Yangpu" single-use venous blood collection needle - Taiwan Registration d0b87316639712db2eb11237ff5e7280

Access comprehensive regulatory information for "Yangpu" single-use venous blood collection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d0b87316639712db2eb11237ff5e7280 and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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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d0b87316639712db2eb11237ff5e7280
Registration Details
Taiwan FDA Registration: d0b87316639712db2eb11237ff5e7280
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Device Details

"Yangpu" single-use venous blood collection needle
TW: โ€œ้™ฝๆ™ฎโ€ไธ€ๆฌกๆ€งไฝฟ็”จ้œ่„ˆๆŽก่ก€้‡
Risk Class 2

Registration Details

d0b87316639712db2eb11237ff5e7280

DHA09200077901

Company Information

Product Details

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

J General hospital and personal use equipment

J.5570 Subcutaneous single-chamber needle

Input;; Chinese goods

Dates and Status

Oct 24, 2016

Oct 24, 2026