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“RUSCHCare” Flocath IntroGel catheters and accessories - Taiwan Registration 30cbdb7be605f567b0fe1fd4fe28023b

Access comprehensive regulatory information for “RUSCHCare” Flocath IntroGel catheters and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30cbdb7be605f567b0fe1fd4fe28023b and manufactured by Teleflex Medical Sdn.Bhd. The authorized representative in Taiwan is TELEFLEX MEDICAL 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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30cbdb7be605f567b0fe1fd4fe28023b
Registration Details
Taiwan FDA Registration: 30cbdb7be605f567b0fe1fd4fe28023b
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Device Details

“RUSCHCare” Flocath IntroGel catheters and accessories
TW: “路希”弗洛凱導引潤滑導尿管及配件
Risk Class 2
MD
Cancelled

Registration Details

30cbdb7be605f567b0fe1fd4fe28023b

Ministry of Health Medical Device Import No. 027667

DHA05602766704

Company Information

Malaysia

Product Details

H Gastroenterology-urology devices

H5130 Urinary catheters and their accessories

Imported from abroad

Dates and Status

Sep 09, 2015

Sep 09, 2020

Jun 07, 2022

Cancellation Information

Logged out

許可證已逾有效期