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“Q-Med”Deflux - Taiwan Registration a7a5571a448052b17dd1d58bf394a436

Access comprehensive regulatory information for “Q-Med”Deflux in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a7a5571a448052b17dd1d58bf394a436 and manufactured by Q-MED AB. The authorized representative in Taiwan is TAIWAN MAJOR CHEMICAL & PHARMACEUTICAL CORP..

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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a7a5571a448052b17dd1d58bf394a436
Registration Details
Taiwan FDA Registration: a7a5571a448052b17dd1d58bf394a436
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Device Details

“Q-Med”Deflux
TW: “科美”逆福仕
Risk Class 3
MD

Registration Details

a7a5571a448052b17dd1d58bf394a436

Department of Health Medical Device Import No. 020258

DHA00602025801

Company Information

Sweden

Product Details

1. Stress-induced urinary incontinence caused by urethral sphincter insufficiency. 2. Vesicoureteral reflux.

H Gastroenterology-urology devices

Imported from abroad

Dates and Status

Oct 27, 2009

Oct 27, 2024