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"Siemens" 800 series 7.3 corrector - Taiwan Registration 55c70638948a7e681198de0b41f697bd

Access comprehensive regulatory information for "Siemens" 800 series 7.3 corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 55c70638948a7e681198de0b41f697bd and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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55c70638948a7e681198de0b41f697bd
Registration Details
Taiwan FDA Registration: 55c70638948a7e681198de0b41f697bd
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Device Details

"Siemens" 800 series 7.3 corrector
TW: โ€œ่ฅฟ้–€ๅญโ€800็ณปๅˆ— 7.3ๆ กๆญฃๅ“
Risk Class 2
Cancelled

Registration Details

55c70638948a7e681198de0b41f697bd

DHA00602181700

Company Information

Product Details

Used in the "Siemens" 800 series blood gas analysis series, it provides single- and two-point correction of pH and electrolytes and zero correction of carbon monoxide module.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Nov 29, 2010

Nov 29, 2020

May 19, 2022

Cancellation Information

Logged out

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