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"Siemens" magnetic resonance imaging instrument - Taiwan Registration e9a4cfaa4c053b0b0960ba0c2927fdab

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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e9a4cfaa4c053b0b0960ba0c2927fdab
Registration Details
Taiwan FDA Registration: e9a4cfaa4c053b0b0960ba0c2927fdab
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Device Details

"Siemens" magnetic resonance imaging instrument
TW: โ€œ่ฅฟ้–€ๅญโ€็ฃๆŒฏ้€ ๅฝฑๅ„€
Risk Class 2

Registration Details

e9a4cfaa4c053b0b0960ba0c2927fdab

DHA05603333300

Company Information

Product Details

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

P Radiology Science

P.1000 ็ฃๆŒฏ่จบๆ–ท่ฃ็ฝฎ

import

Dates and Status

Mar 26, 2020

Mar 26, 2030

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