BEUDAMED
    23 results · 36ms · 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 ×

    3M MINI-DRIVER ELECTRIC SYSTEM

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

    COMPAT ENTERAL DELIVERY SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ELEGANCE GH ELISA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    3 TO 1 REDUCTION DRIVE

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

    3-TO-1 REDUCTION DRIVE

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

    BONE SCR 6.5X30 SELF-TAP

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code MRA·May 28, 2019

    ECHO B-MTRC MP RP SO 8

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 28, 2019

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·February 11, 2013

    RIATA ACTIVE FIXATION

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

    UNKNOWN URETEX MESH PRODUCT

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·July 22, 2014

    CER OPTION TYPE 1 TPR SLEVE -6

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·May 30, 2019

    BONE SCR 6.5X30 SELF-TAP

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code MRA·May 28, 2019

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HTW·May 28, 2019

    G7 PPS LTD ACET SHELL 50D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 28, 2019

    CER OPTION TYPE 1 TPR SLEVE -6

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·May 29, 2019

    ECHO B-MTRC MP RP SO 8

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 28, 2019

    G7 HI-WALL ARCOMXL LNR 36MM D

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 28, 2019

    CER BIOLOXD OPTION HD 36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 28, 2020

    CER OPT TYPE 1 TPR SLEVE 0MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 28, 2020

    BD INSYTE-N¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 25, 2019