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“VACUKANG” Heparin Vacuum Blood Collection Tubes - Taiwan Registration b285ed59f06b49e953f6288b9b6bb239

Access comprehensive regulatory information for “VACUKANG” Heparin Vacuum Blood Collection Tubes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b285ed59f06b49e953f6288b9b6bb239 and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD..

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b285ed59f06b49e953f6288b9b6bb239
Registration Details
Taiwan FDA Registration: b285ed59f06b49e953f6288b9b6bb239
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Device Details

“VACUKANG” Heparin Vacuum Blood Collection Tubes
TW: “永康”肝素真空採血管
Risk Class 2
MD

Registration Details

b285ed59f06b49e953f6288b9b6bb239

Ministry of Health Medical Device Manufacturing No. 005178

Company Information

Taiwan, Province of China

Product Details

It is used to collect blood for clinical laboratory testing of plasma or whole blood.

A Clinical chemistry and clinical toxicology

A1675 Blood Sample Collection Device

Produced in Taiwan, China

Dates and Status

Jun 03, 2016

Jun 03, 2026