"Siemens" multi-faceted magnetic resonance imaging instrument
Taiwan·Risk Class 2·Siemens Healthineers AG, Magnetic Resonance (MR)·Registered Jan 30, 2019 – Jan 30, 2029Active- Analysis ID
- f78f1893d16f2a350a5d4f6e71b4aa37
- Customs Code
- DHA05603210001
- 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
- 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". input
- Registration Date
- Jan 30, 2019
- Expiry Date
- Jan 30, 2029
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Access comprehensive regulatory information for "Siemens" multi-faceted 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 f78f1893d16f2a350a5d4f6e71b4aa37 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, 1 companies making similar products including Siemens Healthineers AG, Magnetic Resonance (MR), and 1 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.