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

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    Filters Regulation: Us FDA ×

    HC Primer

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNTHES BRAINLAB TRAUMA COMPATIBLE INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNEX II

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·April 7, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    APEX HOLE ELIM POSITIVE STOP

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON MEDICAL (DEPUY - SUZHOU) LTD.·Product code MRA·July 11, 2011

    LIBERTY CYCLER

    FDA Adverse Event
    Other ·FRESENIUS MEDICAL CARE·Product code FKX·June 6, 2013

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 10, 2014

    STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·January 10, 2019

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·March 6, 2019

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·February 26, 2019

    CROSSCATH SUPPORT CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·June 20, 2019