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"Siemens" CO2 corrector/diluent - Taiwan Registration e3226c7e9df700e04b4e0c06917894be

Access comprehensive regulatory information for "Siemens" CO2 corrector/diluent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3226c7e9df700e04b4e0c06917894be and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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e3226c7e9df700e04b4e0c06917894be
Registration Details
Taiwan FDA Registration: e3226c7e9df700e04b4e0c06917894be
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Device Details

"Siemens" CO2 corrector/diluent
TW: โ€œ่ฅฟ้–€ๅญโ€ไบŒๆฐงๅŒ–็ขณๆ กๆญฃๅ“/็จ€้‡‹ๆถฒ
Risk Class 2

Registration Details

e3226c7e9df700e04b4e0c06917894be

DHA00602073302

Company Information

Product Details

In vitro diagnostics uses enzyme assays that correct carbon dioxide on different Siemens instruments.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

Contract manufacturing;; input

Dates and Status

Nov 27, 2009

Nov 27, 2029