Taiwan FDA registration bfc112907473ab198253f59ec673f7f6
"HANSON" Silicone Scar Gel (Non-Sterile)
TW: "漢生" 疤痕凝膠 (未滅菌)
Taiwan·Risk Class 1·MD·HANSON MEDICAL INC.·Registered Jun 09, 2015 – Jun 09, 2020CancelledRegistration details
- Analysis ID
- bfc112907473ab198253f59ec673f7f6
- License Form
- Ministry of Health Medical Device Import No. 015315
- Customs Code
- DHA09401531503
Company information
- Manufacturer
- HANSON MEDICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- WEIYOU TECH INC.
Product details
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4025 Scar Treatment Silicone Products
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 09, 2015
- Expiry Date
- Jun 09, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "HANSON" Silicone Scar Gel (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bfc112907473ab198253f59ec673f7f6 and manufactured by HANSON MEDICAL INC.. The authorized representative in Taiwan is WEIYOU TECH INC..
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