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"Yangpu" single-use vacuum blood collection tube (procoagulant tube) - Taiwan Registration aa88873f12721ad38608a5835260ce67

Access comprehensive regulatory information for "Yangpu" single-use vacuum blood collection tube (procoagulant tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa88873f12721ad38608a5835260ce67 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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aa88873f12721ad38608a5835260ce67
Registration Details
Taiwan FDA Registration: aa88873f12721ad38608a5835260ce67
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Device Details

"Yangpu" single-use vacuum blood collection tube (procoagulant tube)
TW: โ€œ้™ฝๆ™ฎโ€ไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(ไฟƒๅ‡็ฎก)
Risk Class 2

Registration Details

aa88873f12721ad38608a5835260ce67

DHA09200062306

Company Information

Product Details

This product is a vacuum container for the collection, storage, transportation and processing of venous blood samples, which can be used for serum clinical chemistry and immunological testing.

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

Chinese goods;; input

Dates and Status

Sep 16, 2014

Sep 16, 2029