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"Siemens" linear accelerator - Taiwan Registration 4ba9fe518e748500ad7467c38ceb31b2

Access comprehensive regulatory information for "Siemens" linear accelerator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ba9fe518e748500ad7467c38ceb31b2 and manufactured by SIEMENS AG MEDICAL SOLUTIONS,BUSINESS UNIT CV. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Siemens AG, Medical Solutions, Business Unit CR Segment RO, SIEMENS AG MEDICAL SOLUTIONS, DIVISION CO, and 2 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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4ba9fe518e748500ad7467c38ceb31b2
Registration Details
Taiwan FDA Registration: 4ba9fe518e748500ad7467c38ceb31b2
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Device Details

"Siemens" linear accelerator
TW: โ€œ่ฅฟ้–€ๅญโ€็›ด็ทšๅŠ ้€Ÿๅ™จ
Risk Class 2
Cancelled

Registration Details

4ba9fe518e748500ad7467c38ceb31b2

DHAS0601993407

Company Information

Product Details

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

P Radiology Science

P.5050 Medical Charged Particle Radiotherapy System

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

Dates and Status

Jun 30, 2009

Jun 30, 2014

Jul 31, 2018

Cancellation Information

Logged out

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