Taiwan FDA registration b3806b15dfc760a70ea36bbb6e3f3fa0

"Siemens" magnetic resonance imaging system

TW: “西門子”磁振造影系統
Taiwan flagTaiwan·Risk Class 2·Siemens Healthineers AG, Magnetic Resonance (MR)·Registered Aug 29, 2019 – Aug 29, 2029Active
Registration details
Analysis ID
b3806b15dfc760a70ea36bbb6e3f3fa0
Customs Code
DHA05603280602
Company information
Manufacturer Country
Germany
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
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
Dates and status
Registration Date
Aug 29, 2019
Expiry Date
Aug 29, 2029
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About this record

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 b3806b15dfc760a70ea36bbb6e3f3fa0 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 SHENZHEN MAGNETIC RESONANCE LTD., 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.

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