"Kemei" reverse Fox
Taiwan·Risk Class 3·Q-MED AB;; Palette Life Sciences·Registered Oct 27, 2009 – Oct 27, 2024Expired- Analysis ID
- 6e77544a9426ef27e6bacc28cbdca6f7
- Customs Code
- DHA00602025801
- Manufacturer
- Q-MED AB;; Palette Life Sciences
- Manufacturer Country
- United States;;Sweden
- Authorized Representative
- TOP GEAL CO., LTD.
- Intended Use
- 1. Stress-induced urinary incontinence caused by urethral sphincter insufficiency. 2. Vesicoureteral reflux.
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- Contract manufacturing;; input
- Registration Date
- Oct 27, 2009
- Expiry Date
- Oct 27, 2024
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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.