Taiwan FDA registration 4a729f326007290a0440c4c28cc0a237
“Keosan” Facial Silicone Implant
TW: “蔻珊”臉部植入物
Taiwan·Risk Class 2·MD·KEOSAN TRADING CO.·Registered Aug 24, 2020 – Aug 24, 2025ExpiredRegistration details
- Analysis ID
- 4a729f326007290a0440c4c28cc0a237
- License Form
- Ministry of Health Medical Device Import No. 033843
- Customs Code
- DHA05603384300
Company information
- Manufacturer
- KEOSAN TRADING CO.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BEAUTYCOM BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3550 Chin Supplement
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 24, 2020
- Expiry Date
- Aug 24, 2025
About this record
Access comprehensive regulatory information for “Keosan” Facial Silicone Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4a729f326007290a0440c4c28cc0a237 and manufactured by KEOSAN TRADING CO.. The authorized representative in Taiwan is BEAUTYCOM BIOTECHNOLOGY CO., 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