BEUDAMED
    1,305 results · 83ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ELECTROSURGICAL COAGULATION FOR AESTHETIC

    FDA Adverse Event
    Injury ·F CARE SYSTEMS USA LLC·Product code ONQ·November 22, 2013

    HOMECHOICE AUTOMATED PD SET W/CASSETTE 4 PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code FKX·November 4, 1998

    SYNERGY

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 13, 2010

    JADA SYSTEM

    FDA Adverse Event
    Injury ·ORGANON & CO.·Product code OQY·February 8, 2024

    HOMECHOICE AUTOMATED PD SET W/CASSETTE 4 PRONG

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code FKX·May 10, 1998

    VANQUISH

    FDA Adverse Event
    Injury ·BTL INDUSTRIES LIMITED·Product code IMJ·September 25, 2015

    SOLETRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·November 15, 2010

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO, JUNCOS·Product code LGW·February 19, 2007

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 24, 2007

    RESTORE ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 13, 2013

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 21, 2025

    VANQUISH

    FDA Adverse Event
    Injury ·BTL INDUSTRIES LIMITED·Product code IMJ·August 18, 2015

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 28, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·December 10, 2009

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO, JUNCOS·Product code LGW·February 27, 2007

    UNKNOWN PUREWICK HOME CARE DISPOSABLE

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code NZU·December 2, 2025

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·March 9, 2007

    PUREWICK MALE EXTERNAL CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD INC. (COVINGTON) -1018233·Product code NZU·October 30, 2025

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·April 15, 2015

    THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·February 18, 2025