FEMTIS® COMFORT POSTERIOR CHAMBER INTRAOCULAR LENS - FDA Registration MDR-08275

Access comprehensive regulatory information for FEMTIS® COMFORT POSTERIOR CHAMBER INTRAOCULAR LENS in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08275 and manufactured by Teleon Surgical B.V - Van Renssenlaerweg 4 b, 6956AV Spankeren. The Netherlands in Netherlands. The device was registered on June 13, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Transmedic 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.