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"Siemens" X-ray system for diagnosis and treatment in urology - Taiwan Registration 971835cc98d26625f6799f9c494a96ca

Access comprehensive regulatory information for "Siemens" X-ray system for diagnosis and treatment in urology in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 971835cc98d26625f6799f9c494a96ca and manufactured by SIEMENS AG, MEDICAL SOLUTIONS, BUSINESS UNIT XP. The authorized representative in Taiwan is SIEMENS HEALTHCARE 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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971835cc98d26625f6799f9c494a96ca
Registration Details
Taiwan FDA Registration: 971835cc98d26625f6799f9c494a96ca
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Device Details

"Siemens" X-ray system for diagnosis and treatment in urology
TW: "่ฅฟ้–€ๅญ" ๆณŒๅฐฟ็ง‘่จบๆ–ทๅŠๆฒป็™‚ๅฐˆ็”จXๅ…‰็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

971835cc98d26625f6799f9c494a96ca

DHAS0601356205

Company Information

Product Details

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

P Radiology Science

P.1650 ้€่ฆ–Xๅ…‰ๅฝฑๅƒๅขžๆ„Ÿ็ฎก

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 18, 2005

Nov 18, 2020

May 19, 2022

Cancellation Information

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