Taiwan FDA registration e553bf70b7e77e4744812e960955b33c
"Siemens" magnetic resonance imaging machine
TW: “西門子”磁共振造影機
Taiwan·Risk Class 2·Siemens Healthineers AG, Magnetic Resonance (MR)·Registered Mar 17, 2014 – Mar 17, 2029ActiveRegistration details
- Analysis ID
- e553bf70b7e77e4744812e960955b33c
- Customs Code
- DHA05602600505
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.1000 磁振診斷裝置
- 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
- Mar 17, 2014
- Expiry Date
- Mar 17, 2029
About this record
Access comprehensive regulatory information for "Siemens" magnetic resonance imaging machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e553bf70b7e77e4744812e960955b33c and manufactured by Siemens Healthineers AG, Magnetic Resonance (MR). The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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