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“SIEMENS” Magnetic Resonance Imaging System - Taiwan Registration 4f8402e0de22191f23f0644f63bc5450

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 4f8402e0de22191f23f0644f63bc5450 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.

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4f8402e0de22191f23f0644f63bc5450
Registration Details
Taiwan FDA Registration: 4f8402e0de22191f23f0644f63bc5450
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Device Details

“SIEMENS” Magnetic Resonance Imaging System
TW: “西門子”磁振造影儀
Risk Class 2
MD

Registration Details

4f8402e0de22191f23f0644f63bc5450

Ministry of Health Medical Device Import No. 032578

DHA05603257802

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

P Devices for radiology

1000

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"

Dates and Status

Apr 19, 2019

Apr 19, 2024

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