"Siemens" magnetic resonance imaging system
Taiwan·Risk Class 2·SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.·Registered May 13, 2016 – May 13, 2021Cancelled- Analysis ID
- 3b24aa95add9e553ef30ca1ac1815860
- Customs Code
- DHA09200076309
- 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 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". Chinese goods;; input
- Registration Date
- May 13, 2016
- Expiry Date
- May 13, 2021
- Cancellation Date
- Aug 04, 2023
- Status
- Logged out
- Reason
- 許可證已逾有效期
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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 3b24aa95add9e553ef30ca1ac1815860 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 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.