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Single-use vacuum blood collection tubes (ESI) - Taiwan Registration 86fe8ee568c19af9df3a26f12277abf4

Access comprehensive regulatory information for Single-use vacuum blood collection tubes (ESI) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 86fe8ee568c19af9df3a26f12277abf4 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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86fe8ee568c19af9df3a26f12277abf4
Registration Details
Taiwan FDA Registration: 86fe8ee568c19af9df3a26f12277abf4
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Device Details

Single-use vacuum blood collection tubes (ESI)
TW: ้™ฝๆ™ฎไธ€ๆฌกๆ€งไฝฟ็”จ็œŸ็ฉบๆŽก่ก€็ฎก(่ก€ๆฒ‰็ฎก)
Risk Class 2

Registration Details

86fe8ee568c19af9df3a26f12277abf4

DHA09200063003

Company Information

Product Details

This product is mainly used for the detection of blood cell sedimentation rate, and the reference method is Wechsler erythrocyte sedimentation rate.

A Clinical chemistry and clinical toxicology

A.1675 Blood collection equipment

Input;; Chinese goods

Dates and Status

Dec 11, 2014

Dec 11, 2029