BEUDAMED
    13 results · 19ms · 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.

    CRYPTO-CEL IF TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    STRATO PLAST PORT INTRO KT(10 FR)LPS 7013/MODIFIED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ACCUPACE GROUP A STREPTOCOCCUS ID TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·August 2, 2012

    SENSOR MODULE LEVEL/BUBBLE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·May 11, 2012

    PI PICC KIT: 2-L 5 FR X 50 CM WITH PRELO

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code LJS·June 25, 2014

    RESERVOIR 3ML

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·February 11, 2013

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·January 6, 2012

    S5 BUBBLE DETECTOR SENSOR 3/16''

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code KRL·February 25, 2022

    STOCKERT S3 LEVEL SENSOR MOUNTING PADS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTW·January 6, 2012

    ALP 501

    FDA Adverse Event
    Injury ·CURRIE MEDICAL SPECIALTIES·Product code JOW·September 1, 2012

    ALP 501

    FDA Adverse Event
    Injury ·CURRIE MEDICAL SPECIALTIES·Product code JOW·July 25, 2012