BEUDAMED
    14 results · 20ms · Sources: EU EUDAMED, US FDA

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    ELECTRONIC SPHYGMOMANOMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Zavation

    FDA UDI
    Zavation LLC·00842166181458·7.5mm Cannullated Tap

    BIOCELLECT

    FDA 510(k)
    FDA Class 2 ·Dental

    BD INTIMA II CLOSED IV CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UNKNOWN IV CATHETER

    FDA Adverse Event
    Injury ·BD (SUZHOU)·Product code FOZ·January 13, 2016

    BD LUER SLIP¿ TUBERCULIN SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMF·February 8, 2018

    TOSHIBA Kalare Diagnostic X-Ray System K110785

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAA·April 3, 2013

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 9, 2013

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FRN·September 23, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·June 1, 2011

    TOSHIBA Kalare Diagnostic X-Ray System K110785

    FDA Enforcement
    Class II ·Terminated·Toshiba American Medical Systems Inc·July 17, 2013

    SYRINGE 5ML LL TIP BULK CONVENIENCE PAK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·January 27, 2021

    Video Duodenoscope

    FDA Enforcement
    Class II ·Terminated·Pentax Medical Company·June 8, 2016

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012