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"Siemens" digital X-ray system - Taiwan Registration 7e2a4b2673c7e61f166655118fc5fe13

Access comprehensive regulatory information for "Siemens" digital X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e2a4b2673c7e61f166655118fc5fe13 and manufactured by SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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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7e2a4b2673c7e61f166655118fc5fe13
Registration Details
Taiwan FDA Registration: 7e2a4b2673c7e61f166655118fc5fe13
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Device Details

"Siemens" digital X-ray system
TW: โ€œ่ฅฟ้–€ๅญโ€ๆ•ธไฝXๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

7e2a4b2673c7e61f166655118fc5fe13

DHAS0602163808

Company Information

Product Details

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

P Radiology Science

P.1680 ๅ›บๅฎšๅผXๅ…‰็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Nov 04, 2010

Nov 04, 2015

Jul 31, 2018

Cancellation Information

Logged out

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