"Kemei" reverse Fox - Taiwan Registration 6e77544a9426ef27e6bacc28cbdca6f7
Access comprehensive regulatory information for "Kemei" reverse Fox in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 6e77544a9426ef27e6bacc28cbdca6f7 and manufactured by Q-MED AB;; Palette Life Sciences. The authorized representative in Taiwan is TOP GEAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Q-MED AB, 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.
Device Details
Registration Details
6e77544a9426ef27e6bacc28cbdca6f7
DHA00602025801
Product Details
1. Stress-induced urinary incontinence caused by urethral sphincter insufficiency. 2. Vesicoureteral reflux.
H Gastroenterology and urology
Contract manufacturing;; input
Dates and Status
Oct 27, 2009
Oct 27, 2024