BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    FLOWERS MEDIAL MALAR IMPLANT

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

    INVENDO C25 COLONOSCOPY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BACTEC MGIT 960 PZA KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    AGC DA2000 KN TIB BRG 71/75X14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·August 31, 2016

    BIOMET AGC V2 INTERLOK TIBIAL 22X 67MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code HRY·June 16, 2017

    AGC V2 INTERLOK TIB 10X 71MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code HRX·May 19, 2017

    SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·January 18, 2013

    NI

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·December 6, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 6, 2014

    AGC V2 INTERLOK TIB 8 X 75MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·April 12, 2017

    AGC V2 INTERLOK TIB 8 X 79MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·March 22, 2016

    AGC REVISION KNEE TIBIAL AUGMENTATION

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code JWH·June 28, 2017