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"Siemens" X-ray system - Taiwan Registration 51140fe66285f4ab6caa4c4f4bc8fcfb

Access comprehensive regulatory information for "Siemens" X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 51140fe66285f4ab6caa4c4f4bc8fcfb 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, 2 companies making similar products including Siemens Healthineers AG, X-Ray Products (XP), SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP, 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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51140fe66285f4ab6caa4c4f4bc8fcfb
Registration Details
Taiwan FDA Registration: 51140fe66285f4ab6caa4c4f4bc8fcfb
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Device Details

"Siemens" X-ray system
TW: โ€œ่ฅฟ้–€ๅญโ€Xๅ…‰็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

51140fe66285f4ab6caa4c4f4bc8fcfb

DHAS0602066608

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

Mar 15, 2010

Mar 15, 2015

Jul 31, 2018

Cancellation Information

Logged out

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