BEUDAMED
    18 results · 23ms · 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 Regulation: Us FDA ×

    DUPONT DIMENSION TOTAL PROTEIN METHOD

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    truFreeze System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CZR PRESS LF STAINS

    FDA 510(k)
    FDA Class 2 ·Dental

    S3 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR)·Product code DTQ·April 23, 2010

    3 TO 1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 14, 2011

    S3 ROLLER PUMP MODULE AND CONSOLE

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR·Product code DTQ·March 24, 2010

    3-TO-1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHMAND·Product code DTQ·December 14, 2011

    STOCKERT S3 CONSOLE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·October 6, 2011

    STOCKERT S3 CONSOLE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·October 6, 2011

    PORTABLE AIR COMPRESSOR FOR MEDICAL PURPOSES

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code BTI·February 8, 2013

    CAPSUREEPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·July 22, 2014

    FREESTYL FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 26, 2007

    SENSOR, LOW LEVEL II

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 16, 2010

    S3 ROLLER PUMP

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND (SORIN GROUP USA, INC. IS DISTRIBUTOR)·Product code DTQ·April 23, 2010

    S3 ROLLER PUMP

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·April 22, 2010

    S3 ROLLER PUMP

    FDA Adverse Event
    SORIN GROUP DEUTSCHLAND·Product code DWB·October 12, 2016

    EQUINOXE, HUMERAL STEM PRIMARY, PRESS FIT 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code HSD·September 9, 2024

    BLOOD CARDIOPLEGIA INSERTS

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTQ·March 24, 2010