Taiwan FDA registration 46cb45d08160b3fc6c66a888f07a28bc
"Pomedon" Silky suspension system
TW: “博美敦”絲蒂懸吊帶系統
Registration details
- Analysis ID
- 46cb45d08160b3fc6c66a888f07a28bc
- Customs Code
- DHA05603316607
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)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3300 Surgical mesh
- Import Information
- import
Dates and status
- Registration Date
- Jan 18, 2020
- Expiry Date
- Jan 18, 2030
About this record
Access comprehensive regulatory information for "Pomedon" Silky suspension system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46cb45d08160b3fc6c66a888f07a28bc 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.
Free DatabasePowered by Pure Global AI89,000+ Devices