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Berecoron undifferentiated heparin correction solution - Taiwan Registration 75d84a5394b1364df7f3d72b3f267404

Access comprehensive regulatory information for Berecoron undifferentiated heparin correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 75d84a5394b1364df7f3d72b3f267404 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..

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75d84a5394b1364df7f3d72b3f267404
Registration Details
Taiwan FDA Registration: 75d84a5394b1364df7f3d72b3f267404
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Device Details

Berecoron undifferentiated heparin correction solution
TW: ๅ€็‘žๅฏ้š†ๆœชๅˆ†ๅŒ–่‚็ด ๆ กๆญฃๆถฒ
Risk Class 2
Cancelled

Registration Details

75d84a5394b1364df7f3d72b3f267404

DHA00602367108

Company Information

Product Details

This product is used as a correction solution for the detection of undifferentiated heparin with the Belikolon heparin reagent.

B Hematology, pathology, and genetics

B.5425 Versatile system for in vitro agglutination studies

import

Dates and Status

Jul 03, 2012

Jul 03, 2022

Apr 12, 2024

Cancellation Information

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