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Deyan centrifuge - Taiwan Registration 07a7baa978df6506f38eb0c3c4e71c4e

Access comprehensive regulatory information for Deyan centrifuge in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 07a7baa978df6506f38eb0c3c4e71c4e and manufactured by DIGISYSTEM LABORATORY INSTRUMENTS INC.. The authorized representative in Taiwan is DIGISYSTEM LABORATORY INSTRUMENTS 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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07a7baa978df6506f38eb0c3c4e71c4e
Registration Details
Taiwan FDA Registration: 07a7baa978df6506f38eb0c3c4e71c4e
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Device Details

Deyan centrifuge
TW: ๅพทๅฝฅ้›ขๅฟƒๆฉŸ
Risk Class 1
Cancelled

Registration Details

07a7baa978df6506f38eb0c3c4e71c4e

DHY04300111103

Company Information

Taiwan, Province of China

Product Details

The volume of red blood cells in the blood is measured by using the quantitative blood separation method to determine whether the total number of red blood cells in the patient is normal.

B Hematology, pathology, and genetics

B.6400 Hemocytometry device

Domestic

Dates and Status

Mar 28, 2006

Mar 28, 2011

Nov 15, 2012

Cancellation Information

Logged out

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