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"Siemens" angiography system - Taiwan Registration 34becf7a8a4042245e844426a1627c32

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 34becf7a8a4042245e844426a1627c32 and manufactured by SIEMENS SHENZHEN MAGNETIC RESONANCE LTD.. 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, 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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34becf7a8a4042245e844426a1627c32
Registration Details
Taiwan FDA Registration: 34becf7a8a4042245e844426a1627c32
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Device Details

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

Registration Details

34becf7a8a4042245e844426a1627c32

DHAS9200063100

Company Information

Product Details

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

P Radiology Science

P.1600 X-ray Vascular Photography System;; P.1650 Fluoroscopic X-ray Sensory Tube

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

Dates and Status

Sep 10, 2014

Sep 10, 2029