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"Siemens" X-ray diagnostic system - Taiwan Registration c93fef9da2cf0ff38094582979bf97b7

Access comprehensive regulatory information for "Siemens" X-ray diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c93fef9da2cf0ff38094582979bf97b7 and manufactured by SIEMENS AG MEDICAL SOLUTIONS, BUSINESS UNIT 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 SHANGHAI MEDICAL EQUIPMENT LTD., SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD.;; Siemens Healthcare GmbH, X-Ray Products (XP), and 3 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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c93fef9da2cf0ff38094582979bf97b7
Registration Details
Taiwan FDA Registration: c93fef9da2cf0ff38094582979bf97b7
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Device Details

"Siemens" X-ray diagnostic system
TW: โ€œ่ฅฟ้–€ๅญโ€Xๅ…‰่จบๆ–ท็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

c93fef9da2cf0ff38094582979bf97b7

DHAS0602427003

Company Information

Product Details

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

P Radiology Science

P.1650 ้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

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 24, 2012

Dec 24, 2017

Nov 04, 2019

Cancellation Information

Logged out

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