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"Medtronic" double-lumen catheter and vascular puncture group - Taiwan Registration 1cd58b754f1ab7d5b697fed1ddf51058

Access comprehensive regulatory information for "Medtronic" double-lumen catheter and vascular puncture group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1cd58b754f1ab7d5b697fed1ddf51058 and manufactured by MC3 Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

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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1cd58b754f1ab7d5b697fed1ddf51058
Registration Details
Taiwan FDA Registration: 1cd58b754f1ab7d5b697fed1ddf51058
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Device Details

"Medtronic" double-lumen catheter and vascular puncture group
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ ้›™่…”ๅฐŽ็ฎกๅŠ่ก€็ฎก็ฉฟๅˆบ็ต„
Risk Class 2

Registration Details

1cd58b754f1ab7d5b697fed1ddf51058

DHA05603743604

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.4100 Long-term respiration/cardiopulmonary insufficiency

import

Dates and Status

Oct 23, 2024

Oct 23, 2029