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“Siemens”Probe for medical use - Taiwan Registration c5640cf41e8ad7bd01b59504ec8cd5c1

Access comprehensive regulatory information for “Siemens”Probe for medical use in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5640cf41e8ad7bd01b59504ec8cd5c1 and manufactured by Siemens Healthineers Ltd.. 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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c5640cf41e8ad7bd01b59504ec8cd5c1
Registration Details
Taiwan FDA Registration: c5640cf41e8ad7bd01b59504ec8cd5c1
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Device Details

“Siemens”Probe for medical use
TW: “西門子”診斷用超音波探頭
Risk Class 2
MD

Registration Details

c5640cf41e8ad7bd01b59504ec8cd5c1

Department of Health Medical Device Import No. 020247

DHA00602024706

Company Information

Korea, Republic of

Product Details

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

P Devices for radiology

P1570 Ultrasound converter for diagnostics

Imported from abroad

Dates and Status

Oct 22, 2009

Oct 22, 2024