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Beckman Coulter IO detects HLA-DR monoclonal antibodies - Taiwan Registration cc71bcb082fcf8b00990b756027d0f87

Access comprehensive regulatory information for Beckman Coulter IO detects HLA-DR monoclonal antibodies in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc71bcb082fcf8b00990b756027d0f87 and manufactured by IMMUNOTECH SAS, A BECKMAN COULTER COMPANY. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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cc71bcb082fcf8b00990b756027d0f87
Registration Details
Taiwan FDA Registration: cc71bcb082fcf8b00990b756027d0f87
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Device Details

Beckman Coulter IO detects HLA-DR monoclonal antibodies
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰นIOๆชขๆธฌHLA-DR ๅ–ฎๆ ชๆŠ—้ซ”
Risk Class 2

Registration Details

cc71bcb082fcf8b00990b756027d0f87

DHA00601755000

Company Information

Product Details

A fluorescently calibrated antibody that uses flow cytometry to identify and count cell populations expressing HLA-DR antigens in human biological samples.

B Hematology, pathology, and genetics

B.5220 Automatic Differentiation Cell Counter

import

Dates and Status

Sep 29, 2006

Sep 29, 2026