BEUDAMED
    25 results · 23ms · Sources: EU EUDAMED, US FDA

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    POSI-GRIP UMBILICAL CORD CLAMP, STERILE, MODEL 384, POSI-GRIP UMBILICAL CORD CLAMP, NON-STERILE, MODEL 385

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526743625·LEVAMED ANKLE SUPPORT SAND V

    Spreader arm - Neonate sternum retractor

    FDA UDI
    Coroneo Inc·00817121000532·Crank-side spreader arm for the neonate sternum...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450096888·

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361010609·PedFuse Reset, SLD, 5.0mm x 35mm

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    IRV2000 INDIVIDUAL RECREATIONAL VEHICLE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    IVS TUNNELLER

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

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

    *

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    CM ALVIM ACQUA IMPLANT 4.3X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·March 16, 2018

    Optetrak Logic

    FDA UDI
    Exactech, Inc.·10885862218933·INSTRUMENT TRAY, LOGIC, RBK, SIZE 3.5

    9616240-2006-00346

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    CERTAS INLIN VLV ONLY W/SPHNGD

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC·Product code JXG·March 19, 2013

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIV.·Product code LGW·March 3, 2011

    RIATA ST OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008

    UNK HIP FEMORAL STEM RECLAIM DISTAL STEM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LPH·November 27, 2023