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Staphylococcus boli rapid latex agglutination kit - Taiwan Registration 41dbe117c08153326e8fe7e4646a6c60

Access comprehensive regulatory information for Staphylococcus boli rapid latex agglutination kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 41dbe117c08153326e8fe7e4646a6c60 and manufactured by PRO-LAB, INC.. The authorized representative in Taiwan is SANCORDON INC..

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41dbe117c08153326e8fe7e4646a6c60
Registration Details
Taiwan FDA Registration: 41dbe117c08153326e8fe7e4646a6c60
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Device Details

Staphylococcus boli rapid latex agglutination kit
TW: ๆณขๅŠ›่‘ก่„็ƒ่Œๅฟซ้€Ÿไนณ่† ๅ‡้›†่ฉฆๅŠ‘็ต„
Risk Class 1
Cancelled

Registration Details

41dbe117c08153326e8fe7e4646a6c60

DHA04400138709

Company Information

Canada

Product Details

Agglutination of staphylococci and latex reagents is used to distinguish Staphylococcus aureus.

C Immunology and microbiology

import

Dates and Status

Oct 28, 2005

Oct 28, 2010

Nov 19, 2012

Cancellation Information

Logged out

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