BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    CHECK VALVE SOLUTION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ILUMIEN OPTIS, DRAGONFLY OPTIS IMAGING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACUMATCH GXL 15DEG LINER 32MM SZ H

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·July 5, 2023

    FORCETRIAD ENERGY PLATFORM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·April 16, 2014

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 4, 2013

    CE INTERMATE, SV 100, 24 PACK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·December 29, 2010

    TFN-ADVANCED Proximal Femoral Nailing System (TFNA); for treatment of fractures in orthopedics and trauma.

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·May 20, 2015