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"Siemens" angiography system - Taiwan Registration 0dfae6fe4776f2b0f847efcfddd82a6c

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 0dfae6fe4776f2b0f847efcfddd82a6c and manufactured by Siemens Healthcare GmbH, 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 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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0dfae6fe4776f2b0f847efcfddd82a6c
Registration Details
Taiwan FDA Registration: 0dfae6fe4776f2b0f847efcfddd82a6c
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Device Details

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

Registration Details

0dfae6fe4776f2b0f847efcfddd82a6c

DHAS5602643104

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

Aug 13, 2014

Aug 13, 2019

May 19, 2022

Cancellation Information

Logged out

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