Dermhage Fullface - ARCSA Registration 0412ed64892c1fb9f1328068a34e9ffb
Access comprehensive regulatory information for Dermhage Fullface in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID 0412ed64892c1fb9f1328068a34e9ffb and manufactured by BOHUS BIOTECH AB. The device was registered on March 21, 2023.
This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.
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ARCSA Official Data
IV
0412ed64892c1fb9f1328068a34e9ffb
Dermhage Fullface
ARCSA ID: 0412ed64892c1fb9f1328068a34e9ffb
Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
Dermhage®
Commercial Name
AUGMENTATION/RECONSTRUCTION IMPLANTS, FACIAL.
Registration Information
Analysis ID
0412ed64892c1fb9f1328068a34e9ffb
Registration Date
March 21, 2023
Expiration Date
March 21, 2028
Product Use
INJECTABLE FACIAL MESOTHERAPY PRODUCT, FOR TREATMENTS OF FINE LINES, SUPERFICIAL WRINKLES AND LIP CORRECTION
Manufacturer
Product Owner
Name
BOHUS BIOTECH AB
Country
SWEDEN
Authorized Representative
Address
BLOCK: 111 VC STREET: AV. FRANCISCO DE ORELLANA SET: GALERIAMILLENIUM NUMBER: S/N INTERSECTION:AV FRANCISCO DE ORELLANA
Phone
2630282