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"KAWASUMI" BLOOD SEPARATOR - Taiwan Registration abb1339979c21c873aeeaa410674c359

Access comprehensive regulatory information for "KAWASUMI" BLOOD SEPARATOR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number abb1339979c21c873aeeaa410674c359 and manufactured by LMB TECHNOLOGIE GMBH. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL 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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abb1339979c21c873aeeaa410674c359
Registration Details
Taiwan FDA Registration: abb1339979c21c873aeeaa410674c359
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Device Details

"KAWASUMI" BLOOD SEPARATOR
TW: "ๅทๆพ„"่‡ชๅ‹•่ก€ๆผฟๅฃ“ๆฟ็ณป็ตฑ
Risk Class 2
MD

Registration Details

abb1339979c21c873aeeaa410674c359

Ministry of Health Medical Device Import No. 030541

DHA05603054105

Company Information

Germany

Product Details

This system is a device used by blood banks and transfusion centers to automatically separate blood components. Red blood cells, plasma, platelets, precipitated brown-yellow layer, frozen precipitate and other components can be separated from whole blood after centrifugation.

B Hematology and pathology devices

B0002 Blood component extraction device

Imported from abroad

Dates and Status

Apr 17, 2018

Apr 17, 2023