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“IMDS” NHancer Guidewire Support Catheter - Taiwan Registration e3e4ecb2aae28f2b928f68d1da15a832

Access comprehensive regulatory information for “IMDS” NHancer Guidewire Support Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3e4ecb2aae28f2b928f68d1da15a832 and manufactured by IMDS Operations B.V.. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., 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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e3e4ecb2aae28f2b928f68d1da15a832
Registration Details
Taiwan FDA Registration: e3e4ecb2aae28f2b928f68d1da15a832
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Device Details

“IMDS” NHancer Guidewire Support Catheter
TW: “迎成”恩施導線支持微細導管
Risk Class 2
MD
Cancelled

Registration Details

e3e4ecb2aae28f2b928f68d1da15a832

Ministry of Health Medical Device Import No. 026584

DHA05602658408

Company Information

Netherlands

Product Details

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Oct 13, 2014

Oct 13, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者