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Vanokan platelet concentrate tube - Taiwan Registration 7f169a836b3f9476fbf0d316cb3943c1

Access comprehensive regulatory information for Vanokan platelet concentrate tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f169a836b3f9476fbf0d316cb3943c1 and manufactured by YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is YUNG KANG MEDICAL DEVICE TECHNOLOGY CO., LTD..

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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7f169a836b3f9476fbf0d316cb3943c1
Registration Details
Taiwan FDA Registration: 7f169a836b3f9476fbf0d316cb3943c1
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Device Details

Vanokan platelet concentrate tube
TW: ๅ‡ก่ซพๅบท่ก€ๅฐๆฟๆฟƒ็ธฎ็ฎก
Risk Class 2

Registration Details

7f169a836b3f9476fbf0d316cb3943c1

Company Information

Taiwan, Province of China

Product Details

This product prepares platelet-rich plasma (PRP) from blood samples.

B Hematology, pathology, and genetics

B.9245 Automated hemocytoseparator

ๅœ‹็”ข;; QMS/QSD

Dates and Status

May 31, 2023

May 31, 2028