Taiwan FDA registration 8d04de81002bc6821ada469bce88140a
"Pomedon" Kelly Star Prolapse Repair System
TW: “博美敦”凱莉星脫垂修補系統
Registration details
- Analysis ID
- 8d04de81002bc6821ada469bce88140a
- Customs Code
- DHA05602698806
Company information
- Manufacturer
- Promedon S.A.
- Manufacturer Country
- Argentina
- Authorized Representative
- Foresee Medical Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.5980 經陰道骨盆腔器官脫垂治療用手術網片
- Import Information
- import
Dates and status
- Registration Date
- Feb 13, 2015
- Expiry Date
- Feb 13, 2025
About this record
Access comprehensive regulatory information for "Pomedon" Kelly Star Prolapse Repair System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8d04de81002bc6821ada469bce88140a and manufactured by Promedon S.A.. The authorized representative in Taiwan is Foresee Medical Ltd..
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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