Pure Global

Profhilo Body 3.2% - 48 mg (H-HA) + 48 mg (L-HA) / 3 mL Hyaluronic acid sodium salt - FDA Registration CMDR-2025-03863

Access comprehensive regulatory information for Profhilo Body 3.2% - 48 mg (H-HA) + 48 mg (L-HA) / 3 mL Hyaluronic acid sodium salt in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03863 and manufactured by IBSA Farmaceutici Italia S.r.l. in Italy. The device was registered on February 04, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Metro Drug, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

Free Database
Powered by Pure Global AI
FDA Official Data
Italy
CMDR-2025-03863
Profhilo Body 3.2% - 48 mg (H-HA) + 48 mg (L-HA) / 3 mL Hyaluronic acid sodium salt
Registered medical device in Philippines
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Information
Product Name
Profhilo Body 3.2% - 48 mg (H-HA) + 48 mg (L-HA) / 3 mL Hyaluronic acid sodium salt
Registration Number
CMDR-2025-03863
Manufacturer Details
Country of Origin
Italy
Importer & Distribution
Importer/Distributor
Metro Drug, Inc.
Registration Dates
Issuance Date
February 04, 2025
Expiry Date
February 04, 2030