Akreos Single-Use Insertion Device - FDA Registration DVR-6480

Access comprehensive regulatory information for Akreos Single-Use Insertion Device in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6480 and manufactured by Bausch & Lomb Inc. 14000 North Goodman Street, Rochester NY 14609, USA Mfd By: Bausch & Lomb Incorporated - 21 N. Park Place Blvd., Clearwater FL 33759, USA in USA. The device was registered on January 09, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Bausch and Lomb Philippines, 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.