Taiwan FDA registration e9a4cfaa4c053b0b0960ba0c2927fdab

"Siemens" magnetic resonance imaging instrument

TW: “西門子”磁振造影儀
Taiwan flagTaiwan·Risk Class 2·Siemens Healthineers AG, Magnetic Resonance (MR)·Registered Mar 26, 2020 – Mar 26, 2030Active
Registration details
Analysis ID
e9a4cfaa4c053b0b0960ba0c2927fdab
Customs Code
DHA05603333300
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
import
Dates and status
Registration Date
Mar 26, 2020
Expiry Date
Mar 26, 2030
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About this record

Access comprehensive regulatory information for "Siemens" magnetic resonance imaging instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e9a4cfaa4c053b0b0960ba0c2927fdab 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, 2 companies making similar products including Siemens Healthineers AG, Magnetic Resonance (MR), SIEMENS SHENZHEN MAGNETIC RESONANCE LTD., and 5 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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