BEUDAMED
    3,166 results · 92ms · 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.

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·August 23, 2018

    CORDUROY DUAL MESH

    FDA Adverse Event
    Injury ·W.L. GORE AND ASSOCIATES·Product code FTL·June 24, 2003

    ARCHITECT HAVAB-G

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code LOL·July 30, 2018

    MEDICATION CASSETTE RESERVOIR/EXTENSION SET ANTI-SIPHON VALV

    FDA Adverse Event
    Malfunction ·*·Product code FPA·September 13, 2005

    MEDICATION CASSETTE RESERVOIR/EXTENSION SET

    FDA Adverse Event
    Malfunction ·*·Product code FPA·September 13, 2005

    ARCHITECT HAVAB-G

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code LOL·July 28, 2020

    ARCHITECT HAVAB-G

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code LOL·September 14, 2018

    ALINITY I HAVAB IGG

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code LOL·July 23, 2018

    MEDICATION CASSETTE/EXTENSION SET W/INTEGRAL ANTI-SIPHON VAL

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL MD, INC·Product code FPA·September 13, 2005

    ARTHREX HEADED BIO-ABSORBABLE CORKSCREW

    FDA Adverse Event
    ARTHREX·Product code MBJ·July 8, 2002

    ARCHITECT ANTI-HBC II

    FDA Adverse Event
    Malfunction ·ABBOTT GERMANY·Product code LOM·May 26, 2017

    CADENCE V-110 SERIES TIERED THERAPY DEFIBRILLATOR

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·January 14, 1999

    CADENCE V-110 SERIES TIERED THERAPOY DEFIBRILLATOR

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·January 14, 1999

    CADENCE V-110 SERIES TIERED THERAPY DEFIBRILLATOR

    FDA Adverse Event
    Death ·ST JUDE MEDICAL INC., CRMD·Product code LWS·January 20, 1999

    CADENCE V-110 SERIES TIERED THERAPY DEFIBRILLATOR

    FDA Adverse Event
    Death ·*·Product code LWS·January 20, 1999

    CADENCE V-110 SERIES TIERED THERAPY DEFIBRILLATOR

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·January 14, 1999

    BI-MET CO-CR HD/NK 13X34X250 R

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 22, 2019

    BI-MET CO-CR HD/NK 13X45X200

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 22, 2019

    BI-MET CO-CR HD/NK 11X45X250 R

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 22, 2019

    REACH 15X250 LT 100% POR FMRL

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·October 22, 2019