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

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    Filters Regulation: Us FDA ×

    Advincula Delineator Uterine Manipulator

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

    THORACIC SUCTION TUBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896000438·THORACIC SUCTION TUBE WITH PYNCHON HANDLE STRAIGHT

    THORACIC SUCTION TUBE

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B0991804290·THORACIC SUCTION TUBE WITH PYNCHON HANDLE STRAIGHT

    MODIFICATON TO: PYRAMID +4 ANTERIOR LUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    URGOCELL AG, ANTIMICROBIAL WOUND DRESSING WITH SILVER

    FDA 510(k)
    FDA Unclassified ·Unknown

    OLYMPUS EMPOWER H65

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·March 20, 2017

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·March 20, 2017

    ELECSYS FT3 III

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CDP·March 20, 2017

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·March 20, 2017

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·February 12, 2017

    ELECSYS FT4 II ASSAY

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·March 21, 2017

    O3 PEDIATRIC SENSOR

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MUD·August 20, 2022

    FT4, FREE THYROXINE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·February 14, 2017

    O3 PEDIATRIC SENSOR

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MUD·August 19, 2022

    COBAS 8000 E 602 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 12, 2017

    MRH KNEE FEM XS RHT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KRO·June 20, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·October 17, 2014