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“Tubex” Super PRP tube system - Taiwan Registration fe27258a597aa4e25fdd5c1e50b81cb8

Access comprehensive regulatory information for “Tubex” Super PRP tube system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fe27258a597aa4e25fdd5c1e50b81cb8 and manufactured by MOOHAN ENTERPRISE CO., LTD.. The authorized representative in Taiwan is Sung Ann Medical Equipment .LTD.

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Registration Details
Taiwan FDA Registration: fe27258a597aa4e25fdd5c1e50b81cb8
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Device Details

“Tubex” Super PRP tube system
TW: “默瀚” 保存血小板濃縮液之容器
Risk Class 2
MD

Registration Details

fe27258a597aa4e25fdd5c1e50b81cb8

Ministry of Health Medical Device Import No. 027897

DHA05602789708

Company Information

Korea, Republic of

Product Details

This product is used to preserve blood and platelet concentrate (PRP) after hemocentrifugation, which can be used for autologous and allogeneic bone mixing surgery.

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Imported from abroad

Dates and Status

Nov 03, 2015

Nov 03, 2025