Taiwan FDA registration d07d9f185158e891c08580a6aac7d697
“Promedon” Vantris VUR Treatment System
TW: “博美敦”範逆勢膀胱輸尿管逆流治療系統
Taiwan·Risk Class 3·MD·Promedon S.A.·Registered May 04, 2021 – May 04, 2026ExpiredRegistration details
- Analysis ID
- d07d9f185158e891c08580a6aac7d697
- License Form
- Ministry of Health Medical Device Import No. 034254
- Customs Code
- DHA05603425409
Company information
- Manufacturer
- Promedon S.A.
- Manufacturer Country
- Argentina
- Authorized Representative
- Foresee Medical Ltd.
Product details
- Intended Use
- This product is used endoscopically to treat vesicoureteral reflux (VUR)
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 04, 2021
- Expiry Date
- May 04, 2026
About this record
Access comprehensive regulatory information for “Promedon” Vantris VUR Treatment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d07d9f185158e891c08580a6aac7d697 and manufactured by Promedon S.A.. The authorized representative in Taiwan is Foresee Medical Ltd..
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