“Siemens” Magnetic Resonance Imaging System
Taiwan·Risk Class 2·MD·SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.·Registered Oct 28, 2019 – May 30, 2028Active- Analysis ID
- 93514acee523a784601870fb7b667b81
- License Form
- Ministry of Health Medical Device Land Transport No. 001080
- Customs Code
- DHA09200108002
- Manufacturer
- SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.
- Manufacturer Country
- China
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1000 Magnetic Resonance Diagnostic Unit
- Import Information
- Imported from abroad; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"
- Registration Date
- Oct 28, 2019
- Expiry Date
- May 30, 2028
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Access comprehensive regulatory information for “Siemens” Magnetic Resonance Imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 93514acee523a784601870fb7b667b81 and manufactured by SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.. 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 Healthcare GmbH, Magnetic Resonance (MR), and 2 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.