Taiwan FDA registration aabd412b5cdd6c4f92eceff6fcbd092f
Activ'M Patch (Non-Sterile)
TW: 愛特恩疤痕護理敷料(未滅菌)
Taiwan·Risk Class 1·MD·M-TECHNOLOGIES·Registered Jan 18, 2018 – Jan 18, 2028ActiveRegistration details
- Analysis ID
- aabd412b5cdd6c4f92eceff6fcbd092f
- License Form
- Ministry of Health Medical Device Import No. 018735
- Customs Code
- DHA09401873501
Company information
- Manufacturer
- M-TECHNOLOGIES
- Manufacturer Country
- France
- Authorized Representative
- GLORIA BIOMED CO., LTD.
Product details
- Intended Use
- Limited to the first-level recognition range of the Measures for the Administration of Medical Devices "Scar Treatment Silicone Products (I.4025)".
- 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
- Jan 18, 2018
- Expiry Date
- Jan 18, 2028
About this record
Access comprehensive regulatory information for Activ'M Patch (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 aabd412b5cdd6c4f92eceff6fcbd092f and manufactured by M-TECHNOLOGIES. The authorized representative in Taiwan is GLORIA BIOMED CO., LTD..
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