JMS ARTERIOVENOUS FISTULA (AVF) NEEDLE SET, FIX TYPE/TWIN - FDA Registration CMDR-2021-00331A

Access comprehensive regulatory information for JMS ARTERIOVENOUS FISTULA (AVF) NEEDLE SET, FIX TYPE/TWIN in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2021-00331A and manufactured by JMS Healthcare Phl, Inc. - Lot 2-B-1, Phase 1B, First Philippine Industrial Park - Special Economic Zone, Tanauan, Batangas in Philippines. The device was registered on December 10, 2021.

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