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

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    C' AIRECUSH SEAT CUSHION

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code FZP·June 7, 2006

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code FZP·June 15, 2006

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code FZP·June 8, 2006

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code FZP·June 7, 2006

    ELECTROSURGICAL DEVICES, 26-0330,26-335,340 & 0345

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

    MAHURKAR DUAL LIMEN FEMORAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PFC C.R. POROUS COATED FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·JOHNSON AND JOHNSON PROFESSIONAL, INC.·Product code HSA·December 11, 1997

    P.F.C. MODULAR KNEE SYSTEM FEMORAL COMPONENT-POROUS

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code HSA·February 3, 1997

    SIGMA CRVD XLK INS 4 8MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code JWH·June 10, 2014

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·December 10, 2012

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 11, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·April 25, 2019

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·April 25, 2019