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“ Elitech” Erythrocyte Sedimentation Rate Test (Non-Sterile) - Taiwan Registration cb22c27c5ee5504d69d3c9a65128369f

Access comprehensive regulatory information for “ Elitech” Erythrocyte Sedimentation Rate Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb22c27c5ee5504d69d3c9a65128369f and manufactured by ELITechGroup B.V.. The authorized representative in Taiwan is Yuxing Enterprise 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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cb22c27c5ee5504d69d3c9a65128369f
Registration Details
Taiwan FDA Registration: cb22c27c5ee5504d69d3c9a65128369f
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Device Details

“ Elitech” Erythrocyte Sedimentation Rate Test (Non-Sterile)
TW: “艾利鐵克” 紅血球沉澱速率試驗(未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

cb22c27c5ee5504d69d3c9a65128369f

Ministry of Health Medical Device Import No. 014952

DHA09401495202

Company Information

Netherlands

Product Details

B Hematology and pathology devices

B6700 Red blood cell sedimentation rate test

Imported from abroad

Dates and Status

Mar 02, 2015

Mar 02, 2020

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者