PORTEX® COMBINED SPINAL/EPIDURAL MINIPACK WITH LOCK, LANCET TIP SPINAL NEEDLE - FDA Registration MDR-05888

Access comprehensive regulatory information for PORTEX® COMBINED SPINAL/EPIDURAL MINIPACK WITH LOCK, LANCET TIP SPINAL NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05888 and manufactured by Smiths Medical ASD, Inc. in United Kingdom. The device was registered on December 06, 2018.

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