Taiwan FDA registration a7a5571a448052b17dd1d58bf394a436
“Q-Med”Deflux
TW: “科美”逆福仕
Taiwan·Risk Class 3·MD·Q-MED AB·Registered Oct 27, 2009 – Oct 27, 2024ExpiredRegistration details
- Analysis ID
- a7a5571a448052b17dd1d58bf394a436
- License Form
- Department of Health Medical Device Import No. 020258
- Customs Code
- DHA00602025801
Company information
- Manufacturer
- Q-MED AB
- Manufacturer Country
- Sweden
- Authorized Representative
- TAIWAN MAJOR CHEMICAL & PHARMACEUTICAL CORP.
Product details
- Intended Use
- 1. Stress-induced urinary incontinence caused by urethral sphincter insufficiency. 2. Vesicoureteral reflux.
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 27, 2009
- Expiry Date
- Oct 27, 2024
About this record
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..
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