“Siemens” Magnetic Resonance Imaging System - Taiwan Registration 93514acee523a784601870fb7b667b81
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 93514acee523a784601870fb7b667b81 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 Healthcare GmbH, Magnetic Resonance (MR), 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.
Device Details
Registration Details
93514acee523a784601870fb7b667b81
Ministry of Health Medical Device Land Transport No. 001080
DHA09200108002
Product Details
For details, it is Chinese approved copy of the imitation order
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
Oct 28, 2019
May 30, 2028
“SIEMENS” Magnetic Resonance Imaging System
Siemens Healthcare GmbH, Magnetic Resonance (MR)
4f8402e0de22191f23f0644f63bc5450
2
“Siemens” Magnetic Resonance Imaging System
Siemens Healthcare GmbH, Magnetic Resonance (MR)
73014c4202ef49c1d0af10a070ca9470
2