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“Siemens” Diagnostic Ultrasound Catheter - Taiwan Registration afa61c602577040ce10e28d493f39ad5

Access comprehensive regulatory information for “Siemens” Diagnostic Ultrasound Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number afa61c602577040ce10e28d493f39ad5 and manufactured by Siemens Healthineers Ltd.. 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 Healthineers Ltd., 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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afa61c602577040ce10e28d493f39ad5
Registration Details
Taiwan FDA Registration: afa61c602577040ce10e28d493f39ad5
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Device Details

“Siemens” Diagnostic Ultrasound Catheter
TW: “西門子” 診斷用超音波導管
Risk Class 2
MD

Registration Details

afa61c602577040ce10e28d493f39ad5

Ministry of Health Medical Device Import No. 034862

DHA05603486206

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E1200 Diagnostic endovascular catheter

Imported from abroad

Dates and Status

Sep 16, 2021

Sep 16, 2026

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