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“Improvacuter” Evacuated Blood Collection Tube (Sodium Heparin Tube) - Taiwan Registration dc1b11f8dd7815335dc3f065d8154f07

Access comprehensive regulatory information for “Improvacuter” Evacuated Blood Collection Tube (Sodium Heparin Tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc1b11f8dd7815335dc3f065d8154f07 and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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dc1b11f8dd7815335dc3f065d8154f07
Registration Details
Taiwan FDA Registration: dc1b11f8dd7815335dc3f065d8154f07
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Device Details

“Improvacuter” Evacuated Blood Collection Tube (Sodium Heparin Tube)
TW: “陽普” 一次性使用真空採血管(肝素鈉管)
Risk Class 2
MD

Registration Details

dc1b11f8dd7815335dc3f065d8154f07

Ministry of Health Medical Device Land Transport No. 000625

DHA09200062500

Company Information

Product Details

It is used to collect blood for plasma biochemical testing in clinical laboratories, and is not suitable for sodium determination.

A Clinical chemistry and clinical toxicology

A1675 Blood Sample Collection Device

Imported from abroad; Made in China

Dates and Status

Sep 25, 2014

Sep 25, 2024