Bioline Leptospira Device - FDA Registration IVDR-00859

Access comprehensive regulatory information for Bioline Leptospira Device in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00859 and manufactured by Abbott Diagnostics Korea Inc. 65, Borahagal-ro, Giheung-gu, Yongin-si, Gyeonggi-do, 19077 Republic of Korea in Korea. The device was registered on June 05, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Allied Hospital Supply International Corporation), 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.