BEUDAMED
    40 results · 24ms · Sources: EU EUDAMED, US FDA

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    XIVE DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Bard® Heyman Follower

    FDA UDI
    C. R. Bard, Inc.·00801741075636·Bard® Heyman Follower

    ULTRAPOWER

    FDA UDI
    Conmed Corporation·10845854001530·ULTRAPOWER BUR, TAPERED (LIME), 3 MM X 36 MM

    CPAP SYSTEM, MODEL 102001

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VENODYNE DVT ADVANTAGE PLUS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOLDSLEEVE W/WINGSCR L55 I-Ø 6 F/LARGE-D

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·January 19, 2023

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012

    HOLDSLEEVE W/WINGSCR L55 I-Ø 6 F/LARGE-D

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·February 7, 2024

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012

    S5 SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

    S5 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012

    S5 SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

    S5 SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

    S5 SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010

    S5 SENSOR MODULE FOR BUBBLE DETECTOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016

    GELPORT LAPAROSCOPIC SYSTEM

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES CORP.·Product code GCJ·March 18, 2013

    HUDSON NEBULIZER W/TEE & TUBING SMALL VOLUME

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code CAF·February 7, 2011

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·March 28, 2008