BEUDAMED
    9 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    AROX 45 JBP

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·November 3, 2006

    PHILOS DR

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO·Product code DTB·November 3, 2006

    PFC SIGMA POSTERIOR LIPPED INSERT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONAL, INC.·Product code JWH·June 18, 1998

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 12, 2024

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·November 16, 2001

    AUTO SUTURE ROTICULATOR 55-4.8

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL CORP·Product code GAG·January 26, 2000

    ARROW/KONTRON 9FR INTRA-AORTIC BALLOON

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code DSP·March 30, 1998

    DREAMSTATION AUTO BIPAP

    FDA Adverse Event
    Injury ·RESPIRONICS, INC·Product code BZD·November 9, 2021

    UNKNOWN NCB PLATE

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HRS·June 11, 2024