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“Arthrex” Angel Blood Processing Set - Taiwan Registration b6ec539d1291b2142d5d8c641165e139

Access comprehensive regulatory information for “Arthrex” Angel Blood Processing Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b6ec539d1291b2142d5d8c641165e139 and manufactured by Arthrex, Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

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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b6ec539d1291b2142d5d8c641165e139
Registration Details
Taiwan FDA Registration: b6ec539d1291b2142d5d8c641165e139
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Device Details

“Arthrex” Angel Blood Processing Set
TW: “艾思瑞斯” 安杰爾血液分離套組
Risk Class 2
MD

Registration Details

b6ec539d1291b2142d5d8c641165e139

Ministry of Health Medical Device Import No. 033510

DHAS5603351004

Company Information

United States

Product Details

This product must be equipped with the "Aceres" Angel platelet thick fluid separation system for the concentration of high-concentration platelet plasma from whole blood or blood bone marrow fluid.

B Hematology and pathology devices

B9245 Automatic Hematology Cell Separator

Imported from abroad

Dates and Status

Jul 22, 2020

Jul 22, 2025