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"Siemens" angiography system - Taiwan Registration 6218de523b57d5d936bf7443772bc3db

Access comprehensive regulatory information for "Siemens" angiography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6218de523b57d5d936bf7443772bc3db and manufactured by Siemens Healthineers AG, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including Siemens Healthineers AG, Advanced Therapies, Siemens Healthcare GmbH, Advanced Therapies, 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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6218de523b57d5d936bf7443772bc3db
Registration Details
Taiwan FDA Registration: 6218de523b57d5d936bf7443772bc3db
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Device Details

"Siemens" angiography system
TW: โ€œ่ฅฟ้–€ๅญโ€่ก€็ฎกๆ”ๅฝฑ็ณป็ตฑ
Risk Class 2

Registration Details

6218de523b57d5d936bf7443772bc3db

DHAS5602927709

Company Information

Product Details

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

P Radiology Science

P.1600 Xๅ…‰่ก€็ฎกๆ”ๅฝฑ็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Jan 11, 2017

Jan 11, 2027