BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    PRESTIGE AMERITECH FACE MASK

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    REDON SET

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    THE UNI-CLIP STAPLE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN NOTTINGHAM SHOULDER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code MBF·May 17, 2017

    COMPREHENSIVE SHOULDER SYSTEM MODULAR HEAD - VARIABLE OFFSET 42MM X 18MM X 46MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HSD·October 19, 2016

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·March 29, 2013

    BIO-PUSHLOCK 3.5MM X 14MM

    FDA Adverse Event
    Other ·ARTHREX, INC.·Product code MAI·June 13, 2008

    BIOMET/SURGICAL SPECIALITES

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code LPH·April 13, 2011

    CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.

    FDA Enforcement
    Class II ·Terminated·Smiths Medical ASD, Inc.·June 24, 2015