“Siemens” Magnetic Resonance Imaging System
Taiwan·Risk Class 2·MD·Siemens Healthcare GmbH, Magnetic Resonance (MR)·Registered Jan 18, 2017 – May 30, 2023Cancelled- Analysis ID
- 73014c4202ef49c1d0af10a070ca9470
- License Form
- Ministry of Health Medical Device Import No. 029287
- Customs Code
- DHA05602928704
- Manufacturer
- Siemens Healthcare GmbH, Magnetic Resonance (MR)
- Manufacturer Country
- Germany
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
- 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
- Jan 18, 2017
- Expiry Date
- May 30, 2023
- Cancellation Date
- Jan 17, 2020
- Status
- Logged out
- Reason
- 自請註銷
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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 73014c4202ef49c1d0af10a070ca9470 and manufactured by Siemens Healthcare GmbH, 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 Healthcare GmbH, Magnetic Resonance (MR), SIEMENS SHENZHEN MAGNETIC RESONANCE LTD., 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.