Taiwan FDA registration 50f40c298b588aa7e855b4d552f6ba04
"Siemens" positron magnetic resonance imaging instrument
TW: “西門子”正子磁振造影儀
Taiwan·Risk Class 2·Siemens Healthineers AG, Magnetic Resonance (MR)·Registered Jan 11, 2012 – Jan 11, 2027ActiveRegistration details
- Analysis ID
- 50f40c298b588aa7e855b4d552f6ba04
- Customs Code
- DHA00602319107
Company information
- Manufacturer
- Siemens Healthineers AG, Magnetic Resonance (MR)
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1200 Radiology CT system
- Import Information
- 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
- Registration Date
- Jan 11, 2012
- Expiry Date
- Jan 11, 2027
About this record
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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