Reuter Bivalve, Fluoroplastic Internasal Splint, No Split - SFDA Registration ME0000000294SFDAA00087
Access comprehensive regulatory information for Reuter Bivalve, Fluoroplastic Internasal Splint, No Split in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000000294SFDAA00087 and manufactured by Medtronic XOMED, Inc.
This page provides complete registration details including product category (MD), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
Invasive Implants Device
Medtronic Internal Nasal Splints are indicated for use with nasal surgery or trauma.
[]

