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"Siemens" linear accelerator - Taiwan Registration 12df4185cb00efb784c443b794e54410

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 12df4185cb00efb784c443b794e54410 and manufactured by SIEMENS AG MEDICAL SOLUTIONS, DIVISION CO. 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, Business Unit CR Segment RO, 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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12df4185cb00efb784c443b794e54410
Registration Details
Taiwan FDA Registration: 12df4185cb00efb784c443b794e54410
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Device Details

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

Registration Details

12df4185cb00efb784c443b794e54410

DHAS0602068805

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

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

Mar 23, 2010

Mar 23, 2015

Jul 31, 2018

Cancellation Information

Logged out

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