Taiwan FDA registration 879624389f064e84f657e6686b2851ed
Activ'M Gel (Non-Sterile)
TW: 愛特恩疤痕護理凝膠(未滅菌)
Registration details
- Analysis ID
- 879624389f064e84f657e6686b2851ed
- License Form
- Ministry of Health Medical Device Import No. 018838
- Customs Code
- DHA09401883801
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
- Feb 27, 2018
- Expiry Date
- Feb 27, 2028
About this record
Access comprehensive regulatory information for Activ'M 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 879624389f064e84f657e6686b2851ed and manufactured by M-TECHNOLOGIES. The authorized representative in Taiwan is GLORIA BIOMED 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