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"Siemens" mobile X-ray system - Taiwan Registration 5ab80a683de141c6f106a5a3d0ee897b

Access comprehensive regulatory information for "Siemens" mobile X-ray system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ab80a683de141c6f106a5a3d0ee897b and manufactured by Siemens Healthineers AG, Advanced Therapies. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIEMENS LTD. MEDICAL SOLUTIONS DIVISION GOA WORKS, and 1 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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5ab80a683de141c6f106a5a3d0ee897b
Registration Details
Taiwan FDA Registration: 5ab80a683de141c6f106a5a3d0ee897b
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Device Details

"Siemens" mobile X-ray system
TW: โ€œ่ฅฟ้–€ๅญโ€ ็งปๅ‹•ๅผXๅ…‰็ณป็ตฑ
Risk Class 2

Registration Details

5ab80a683de141c6f106a5a3d0ee897b

DHAS5603744908

Company Information

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.1720 ็งปๅ‹•ๅผXๅ…‰็ณป็ตฑ

The consent of the Nuclear Safety Commission must be obtained for each import of this medical device.;; input

Dates and Status

Oct 31, 2024

Oct 31, 2029

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