"Siemens" magnetic resonance imaging instrument
Taiwan·Risk Class 2·Siemens Healthineers AG, Magnetic Resonance (MR)·Registered Aug 01, 2017 – Aug 01, 2027Active- Analysis ID
- 25d9d39c16a98a5e18c0983a2e97a80a
- Customs Code
- DHA05602999403
- Manufacturer
- Siemens Healthineers AG, Magnetic Resonance (MR)
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- 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.
- Registration Date
- Aug 01, 2017
- Expiry Date
- Aug 01, 2027
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Access comprehensive regulatory information for "Siemens" 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 25d9d39c16a98a5e18c0983a2e97a80a and manufactured by Siemens Healthineers AG, Magnetic Resonance (MR). The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Siemens Healthineers AG, Magnetic Resonance (MR), SIEMENS SHENZHEN MAGNETIC RESONANCE LTD., and 5 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.