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"Siemens" positron magnetic resonance imaging instrument - Taiwan Registration 50f40c298b588aa7e855b4d552f6ba04

Access comprehensive regulatory information for "Siemens" positron magnetic resonance imaging instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50f40c298b588aa7e855b4d552f6ba04 and manufactured by Siemens Healthineers AG, Magnetic Resonance (MR). The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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50f40c298b588aa7e855b4d552f6ba04
Registration Details
Taiwan FDA Registration: 50f40c298b588aa7e855b4d552f6ba04
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Device Details

"Siemens" positron magnetic resonance imaging instrument
TW: โ€œ่ฅฟ้–€ๅญโ€ๆญฃๅญ็ฃๆŒฏ้€ ๅฝฑๅ„€
Risk Class 2

Registration Details

50f40c298b588aa7e855b4d552f6ba04

DHA00602319107

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1200 Radiology CT system

Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Jan 11, 2012

Jan 11, 2027