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

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    Filters Regulation: Us FDA ×

    VEGA Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·December 4, 2002

    CHLORASHIELD TM ANTIMICROBIAL DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    PINN-ACL CROSSPIN

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRULIANT KNEE COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 22, 2024

    DIMENSION(R) CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code LCP·June 3, 2013

    AXXESS PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 23, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015

    Mallinckrodt Satin-Slip Intubation Stylet, 6 Fr., single use, Model number 85863,shipped in cases of 20

    FDA Recall
    Terminated ·Nellcor Puritan Bennett·Product code BSR·July 12, 2006