BEUDAMED
    15 results · 46ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    BIOPRO, INC.

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code HSH·November 30, 1999

    BIOPRO PSL FEMORAL HIP STEM

    FDA Adverse Event
    Malfunction ·BIOPRO INC.·Product code KWY·June 14, 2012

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    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code HSH·June 23, 1999

    BIOPRO

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code HSH·January 5, 2000

    BIOPRO

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code HSH·January 6, 2000

    BIOPRO

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code MVB·April 24, 2003

    BIOPRO SUBTALAR IMPLANT

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code NDL·July 23, 2009

    BIOPRO MEMORY STAPLE

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code GDW·October 15, 2012

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    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code KWY·May 29, 2011

    TOTAL KNEE IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code JWH·November 30, 1999

    GO-EZ

    FDA Adverse Event
    Malfunction ·BIOPRO, INC·Product code HWC·August 9, 2016

    BIOPRO MEMORY STAPLE

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code GDW·November 29, 2007

    BIOPRO PSL HIP STEM

    FDA Adverse Event
    Malfunction ·BIOPRO INC·Product code LPH·October 26, 2015

    TOTAL JOINT PROSTHESIS, FEMORAL STEM

    FDA Adverse Event
    Malfunction ·BIOPRO, INC.·Product code KWY·March 29, 1996

    BIOPRINCE NEEDLE

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES INC.·Product code KNW·September 11, 2019