Philips IntelliSite Pathology Solution 5.1 - FDA Registration 252d48957bb145807b7755b569a1b11e

Access comprehensive regulatory information for Philips IntelliSite Pathology Solution 5.1 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 252d48957bb145807b7755b569a1b11e and manufactured by Philips Medical Systems Nederland B.V.. The device was registered on November 09, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.