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"Siemens" linear accelerator - Taiwan Registration fc20d1d766cdf343cd2d940b78e37c22

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 fc20d1d766cdf343cd2d940b78e37c22 and manufactured by Siemens AG, Medical Solutions, Business Unit CR Segment RO. 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 CV, 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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Registration Details
Taiwan FDA Registration: fc20d1d766cdf343cd2d940b78e37c22
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Device Details

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

Registration Details

fc20d1d766cdf343cd2d940b78e37c22

DHAS0601291609

Company Information

Product Details

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

P Radiology Science

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

Nov 03, 2005

Nov 03, 2015

Jul 31, 2018

Cancellation Information

Logged out

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