BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    ETHICON PHYSIOMESH OPEN FLEXIBLE COMPOSITE MESH DEVICE

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

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694046640·PrimaLIF LLIF PEEK Implant, 15mm X 26mm X 60mm,...

    Canaveral®

    FDA UDI
    FLOSPINE LLC·B183114150600·Monoaxial Screw, 10.5mm x 60mm

    FLO-ASSISTANT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MEDLINE RETRACTABLE SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code LZG·April 11, 2016

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·June 27, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 4, 2014

    ZIMMER DISTAL FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 26, 2017

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·March 19, 2015

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·March 19, 2015