BEUDAMED
    10,000 results · 42ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    SURGISTOOL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FZM·October 21, 2015

    EnSite™

    FDA UDI
    ST. JUDE MEDICAL, INC.·05415067031730·X EP System Catheter Connector Cable

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·07613327601329·EP Catheter Cable, 10 pins

    VELA VENTILATOR

    FDA Adverse Event
    Malfunction ·VYAIRE MEDICAL·Product code CBK·November 19, 2020

    PRECISION SPECTRA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 18, 2024

    ACCUPLAN

    FDA Adverse Event
    Malfunction ·MEDCAD·Product code NDP·May 19, 2021

    MESHGRAFT II COMPLETE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·November 9, 2018

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Injury ·DEXCOM, INC.·Product code QBJ·March 16, 2021

    N/A

    FDA UDI
    INNOVATIVE HEALTH LLC·10841898132452·EnSite X EP System Catheter Connector Cable, 36...

    UNKNOWN COOLSCULPTING SYSTEM

    FDA Adverse Event
    Injury ·ALLERGAN PLEASANTON·Product code OOK·June 22, 2023

    UNKNOWN COOLSCULPTING® SYSTEM

    FDA Adverse Event
    Injury ·ALLERGAN PLEASANTON·Product code OOK·June 22, 2023

    HOD ENHCD INS 32/49 APR

    FDA Adverse Event
    Injury ·CENTERPULSE ORTHOPEDICS, INC.·Product code KWB·November 10, 2003

    HOD ENHCD INS 28/45 APR

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·July 26, 2000

    SX28MM/57MM HOD INS INTER-OP

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code LPH·June 2, 2000

    SZ28MM/57MM HOD INS INTER-OP

    FDA Adverse Event
    Injury ·ZIMMER AUSTIN, INC.·Product code LPH·July 22, 2004

    HOD ENHCD INS 28/49 APR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 27, 2018

    HOD ENHCD INS 28/57 APR

    FDA Adverse Event
    Injury ·CENTERPLUS ORTHOPEDICS, INC·Product code KWB·January 31, 2003

    HOD ENHCD INS 32/55 APR

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·July 30, 2002

    HOD ENHCD INS 32/55 APR

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·December 3, 2001

    SZ22MM/49MM HOD INS INTER-OP

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code LPH·November 15, 2001