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"Siemens" angiography system - Taiwan Registration 3905013e162bf15b99864f54f887aace

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 3905013e162bf15b99864f54f887aace 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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3905013e162bf15b99864f54f887aace
Registration Details
Taiwan FDA Registration: 3905013e162bf15b99864f54f887aace
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Device Details

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

Registration Details

3905013e162bf15b99864f54f887aace

DHAS5603532901

Company Information

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.1600 Xๅ…‰่ก€็ฎกๆ”ๅฝฑ็ณป็ตฑ

Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Mar 15, 2022

Mar 15, 2027