BEUDAMED
    9 results · 21ms · 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 ×

    MEDTRONIC EXTENDED

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 23, 2025

    INSET GUARD

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·May 5, 2026

    LIGACLIP ROTATING MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.·Product code GDO·June 20, 1997

    ENDOPATH DILATING TIP TROCAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·June 20, 1997

    HDI 5000 ULTRASOUND STANDARD SYSTEM

    FDA Adverse Event
    Malfunction ·PHILIPS ULTRASOUND, INC.·Product code IYO·March 30, 2012

    ENDOPATH OPTIVIEW SURG. OPTICAL OBTURATOR & SLEEVE

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·June 20, 1997

    RESTORE SENSOR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 19, 2013

    NEOPUFF INFANT RESUSCITATOR

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTL·March 8, 2011

    HAKIM PROG VALVE INLINE SIPHONGUARD

    FDA Adverse Event
    Death ·CODMAN & SHURTLEFF, INC/MEDOS S.A.·Product code JXG·March 11, 2008