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“SEAWON” Autologous Platelet Rich Plasma Kit - Taiwan Registration 32c249456630dc16ff2ab80e69d0f69d

Access comprehensive regulatory information for “SEAWON” Autologous Platelet Rich Plasma Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 32c249456630dc16ff2ab80e69d0f69d and manufactured by Seawon Meditech Co., Ltd.. The authorized representative in Taiwan is SINCERE BIOTECH CO., LTD..

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32c249456630dc16ff2ab80e69d0f69d
Registration Details
Taiwan FDA Registration: 32c249456630dc16ff2ab80e69d0f69d
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Device Details

“SEAWON” Autologous Platelet Rich Plasma Kit
TW: “希旺” 血小板濃厚液自動分離組
Risk Class 2
MD

Registration Details

32c249456630dc16ff2ab80e69d0f69d

Ministry of Health Medical Device Import No. 029191

DHA05602919104

Company Information

Korea, Republic of

Product Details

This product isolates platelet thick fluid from blood samples and is used in mixed bone surgery for autologous and allogeneic grafts.

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Imported from abroad

Dates and Status

Jan 16, 2017

Jan 16, 2022