BEUDAMED
    14 results · 19ms · Sources: EU EUDAMED, US FDA

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    VESSELOOPS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    EQUISTREAM Long-Term Hemodialysis Catheter

    FDA UDI
    Bard Access Systems, Inc.·00801741013805·EQUISTREAM HEMODIALYSIS CATH, ALPHACURVE, AIRGU...

    DISTRACTION, INTERNAL

    FDA UDI
    KLS-Martin L.P.·00888118093073·ACT ARM, RIGID, REMOTE DETACH, CONCEALED TIP, T...

    BD PLASTIPAK CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 11, 2020

    ASTEL NON-METAL BACKED ACETABULAR CUP FOR CEMENTED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DELFIA TBG KIT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BD PLASTIPAK 50ML LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 10, 2019

    BD DISCARDIT II 20 ML SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 30, 2019

    MW5043863

    FDA Adverse Event
    Injury ·July 10, 2015

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·January 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·July 1, 2014

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JGS·February 21, 2012

    EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product code:5905240, 14.5 Fr. Alphacurve Catheter with Standard Kit, 24cm length, BARD, UDI# 00801741013805

    FDA Enforcement
    Class II ·Terminated·Bard Peripheral Vascular Inc·September 4, 2019

    EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product code:5905240, 14.5 Fr. Alphacurve Catheter with Standard Kit, 24cm length, BARD, UDI# 00801741013805

    FDA Recall
    Terminated ·Bard Peripheral Vascular Inc·Product code MSD·May 31, 2019