Biopsy Needle Kit - SFDA Registration ME0000000301SFDAA00239
Access comprehensive regulatory information for Biopsy Needle Kit in the Saudi Arabia medical device market through Pure Global AI's free database. This Class III device is registered with Saudi Arabia SFDA under registration number ME0000000301SFDAA00239 and manufactured by Medtronic Navigation, Inc..
This page provides complete registration details including product category (Medical Device), 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.
Single Use Passive Needle Kit
The Biopsy Needle is a presterilized, single-use, side-cutting needle for cranial tissue biopsies. Rotation of an inner cannula within an outer cannula provides the cutting action.
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