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“Siemens” Magnetic Resonance Imaging System - Taiwan Registration 73014c4202ef49c1d0af10a070ca9470

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.

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73014c4202ef49c1d0af10a070ca9470
Registration Details
Taiwan FDA Registration: 73014c4202ef49c1d0af10a070ca9470
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Device Details

“Siemens” Magnetic Resonance Imaging System
TW: “西門子”核磁共振影像系統
Risk Class 2
MD
Cancelled

Registration Details

73014c4202ef49c1d0af10a070ca9470

Ministry of Health Medical Device Import No. 029287

DHA05602928704

Company Information

Product Details

P Devices for radiology

P1000 Magnetic Resonance Diagnostic Unit

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

Jan 18, 2017

May 30, 2023

Jan 17, 2020

Cancellation Information

Logged out

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