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"Siemens" X-ray post-processing working system - Taiwan Registration c8b0d402d4ed2d11ab460ed740de5d02

Access comprehensive regulatory information for "Siemens" X-ray post-processing working system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c8b0d402d4ed2d11ab460ed740de5d02 and manufactured by Siemens Healthcare GmbH, Advanced Therapies. 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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c8b0d402d4ed2d11ab460ed740de5d02
Registration Details
Taiwan FDA Registration: c8b0d402d4ed2d11ab460ed740de5d02
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Device Details

"Siemens" X-ray post-processing working system
TW: "่ฅฟ้–€ๅญ"Xๅ…‰ๅพŒ่™•็†ๅทฅไฝœ็ณป็ตฑ
Risk Class 2

Registration Details

c8b0d402d4ed2d11ab460ed740de5d02

DHA00601434507

Company Information

Product Details

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

P Radiology Science

import

Dates and Status

Apr 24, 2006

Apr 24, 2026