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Shakessell blood rate sedimentation test equipment - Taiwan Registration 9595bacfdde6cdefb9d088d29948c708

Access comprehensive regulatory information for Shakessell blood rate sedimentation test equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9595bacfdde6cdefb9d088d29948c708 and manufactured by SARSTEDT AG & CO.. The authorized representative in Taiwan is PAN ASIA BIOMEDICAL TECHNOLOGY INC..

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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9595bacfdde6cdefb9d088d29948c708
Registration Details
Taiwan FDA Registration: 9595bacfdde6cdefb9d088d29948c708
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Device Details

Shakessell blood rate sedimentation test equipment
TW: ่ŽŽไป•ๅพท่ก€ๆถฒ้€Ÿ็އๆฒ‰้™ๆธฌ่ฉฆๅ™จๆ
Risk Class 1
Cancelled

Registration Details

9595bacfdde6cdefb9d088d29948c708

DHA04400200602

Company Information

Germany

Product Details

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B Hematology, pathology, and genetics

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import

Dates and Status

Nov 17, 2005

Nov 17, 2015

Aug 14, 2018

Cancellation Information

Logged out

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