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"Siemens" automatic urine analyzer correction solution group - Taiwan Registration d38507efe8535802700f3dbc944a4329

Access comprehensive regulatory information for "Siemens" automatic urine analyzer correction solution group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d38507efe8535802700f3dbc944a4329 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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d38507efe8535802700f3dbc944a4329
Registration Details
Taiwan FDA Registration: d38507efe8535802700f3dbc944a4329
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Device Details

"Siemens" automatic urine analyzer correction solution group
TW: โ€œ่ฅฟ้–€ๅญโ€ๅ…จ่‡ชๅ‹•ๅฐฟๆถฒๅˆ†ๆžๅ„€ ๆ กๆญฃๆถฒ็ต„
Risk Class 2

Registration Details

d38507efe8535802700f3dbc944a4329

DHA00602154101

Company Information

Product Details

THIS CORRECTION SOLUTION IS USED IN CONJUNCTION WITH CLINITEK TLAS REAGENTS TO CORRECT THE FULLY AUTOMATED URINE ANALYZER CLINITEK ATLAS.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Sep 16, 2010

Sep 16, 2025