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"Siemens" diagnostic X-ray machine - Taiwan Registration 20c942d18859f93291fc758c58efd6f2

Access comprehensive regulatory information for "Siemens" diagnostic X-ray machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 20c942d18859f93291fc758c58efd6f2 and manufactured by Siemens Healthcare GmbH, X-Ray Products (XP). 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 AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP, Siemens Healthcare GmbH;; SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD., and 4 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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20c942d18859f93291fc758c58efd6f2
Registration Details
Taiwan FDA Registration: 20c942d18859f93291fc758c58efd6f2
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Device Details

"Siemens" diagnostic X-ray machine
TW: โ€œ่ฅฟ้–€ๅญโ€่จบๆ–ทๅž‹Xๅ…‰ๆฉŸ
Risk Class 2
Cancelled

Registration Details

20c942d18859f93291fc758c58efd6f2

DHAS5603307206

Company Information

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

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

Dec 20, 2019

Nov 06, 2022

Apr 12, 2024

Cancellation Information

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