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“YK” Platelet-Rich Plasma Concentrate Kit - Taiwan Registration e47a2dfc5ecf50bc65c04df17e4f4f11

Access comprehensive regulatory information for “YK” Platelet-Rich Plasma Concentrate Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e47a2dfc5ecf50bc65c04df17e4f4f11 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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e47a2dfc5ecf50bc65c04df17e4f4f11
Registration Details
Taiwan FDA Registration: e47a2dfc5ecf50bc65c04df17e4f4f11
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Device Details

“YK” Platelet-Rich Plasma Concentrate Kit
TW: “永康”血小板濃縮器
Risk Class 2
MD

Registration Details

e47a2dfc5ecf50bc65c04df17e4f4f11

Ministry of Health Medical Device Manufacturing No. 005633

Company Information

Taiwan, Province of China

Product Details

This product can be isolated from blood samples to prepare platelet-rich plasma (PRP). When clinically indicated, platelet thick fluid can be used for mixed autologous and allogeneic orthopedic surgery.

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Produced in Taiwan, China

Dates and Status

Aug 09, 2017

Aug 09, 2027