BEUDAMED
    9 results · 20ms · 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 FDA Adverse Event ×

    PROTECTA XT CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 5, 2015

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 21, 2013

    UNK JUVEDERM VOLUMA

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·July 8, 2014

    MONOSYN QUICK

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·May 20, 2022

    DAVINCI XI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·November 25, 2024

    MONOMEND ST 4/0 18''(45CM) HR17 VPL .RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·May 5, 2026

    MONOMEND ST5/0 18"(45CM)DSMP11(M)VPL.RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·January 2, 2023

    MONOMEND ST5/0 18"(45CM)DSMP11(M)VPL.RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·January 2, 2023

    MONOMEND ST 5/0 18''(45)DSMP13(M)VPL.RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·March 25, 2026