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

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    SCIMED 6 FRENCH IMPULSE ANGIOGRAPHIC CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    QUALTEX SKIN MARKER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    BABYFLEX PATIENT CIRCUIT

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PSO KNEE BONE SUBSTITUTION

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRO·April 22, 2022

    1.5MM RESORB ORBITAL FLOOR PL 24MMX24MM W/BENDING TEMP-STER

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·November 2, 2012

    PSO KNEE BONE SUBSTITUTION

    FDA Adverse Event
    Injury ·BIOMET SPAIN, S.L.·Product code KRO·July 18, 2019

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 3, 2014

    UNKNOWN HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 16, 2018

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 31, 2025