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“Siemens” Diagnostic Ultrasound Catheter - Taiwan Registration ae2207fd7d7c4a336929413ecd3bc75b

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 ae2207fd7d7c4a336929413ecd3bc75b 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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ae2207fd7d7c4a336929413ecd3bc75b
Registration Details
Taiwan FDA Registration: ae2207fd7d7c4a336929413ecd3bc75b
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Device Details

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

Registration Details

ae2207fd7d7c4a336929413ecd3bc75b

Ministry of Health Medical Device Import No. 025649

DHA05602564905

Company Information

Korea, Republic of

Product Details

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

E Cardiovascular devices

E1200 Diagnostic endovascular catheter

Imported from abroad

Dates and Status

Dec 02, 2013

Dec 02, 2023

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