BEUDAMED
    328 results · 24ms · 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 Status: Injury ×

    SBI - SMALL BONE INNOVATIONS

    FDA Adverse Event
    Injury ·SBI·Product code KWI·April 1, 2008

    PRIDE MOBILITY PRODUCTS

    FDA Adverse Event
    Injury ·PRIDE MOBILITY PRODUCTS·Product code ITI·June 9, 2023

    SURDIAL DX HEMODIALYSIS SYSTEM AND ACCESSORIES

    FDA Adverse Event
    Injury ·SHIBUYA (SBY)·Product code KDI·May 23, 2022

    SURDIAL DX HEMODIALYSIS SYSTEM AND ACCESSORIES

    FDA Adverse Event
    Injury ·SHIBUYA (SBY)·Product code KDI·May 23, 2022

    NIPRO SURDIAL DX HEMODIALYSIS SYSTEM

    FDA Adverse Event
    Injury ·SHIBUYA (SBY)·Product code KDI·October 11, 2021

    SURDIAL X

    FDA Adverse Event
    Injury ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Injury ·SHIBUYA (SBY)·Product code KDI·August 4, 2021

    SURDIAL X

    FDA Adverse Event
    Injury ·SHIBUYA (SBY)·Product code KDI·August 6, 2021

    SURDIAL X

    FDA Adverse Event
    Injury ·SHIBUYA (SBY)·Product code KDI·August 4, 2021

    COMPOSITCP INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SBM SAS·Product code MAI·July 13, 2017

    COMPOSITCP INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SBM S.A.S.·Product code HWC·January 23, 2015

    00430829

    FDA Adverse Event
    Injury ·BETA BIONICS INC·Product code QFG·October 17, 2025

    10MM TI CANN TIBIAL NAIL-EX W/PROX BEND 375MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES PRODUKTIONS GMBH·Product code JDS·July 21, 2021

    POLYAXIAL SCREW (DIA. 3.5 MM X 14 MM L)

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWP·October 3, 2022

    ILET BIONIC PANCREAS

    FDA Adverse Event
    Injury ·BETA BIONICS, INC.·Product code QFG·September 21, 2025

    THERASPHERE 5 GBQ

    FDA Adverse Event
    Injury ·MDS NORDION·Product code KXK·January 17, 2002

    THERASPHERE 20 GBQ

    FDA Adverse Event
    Injury ·MDS NORDION, INC.·Product code KXK·March 6, 2001

    THERASPHERE 10 GBQ

    FDA Adverse Event
    Injury ·MDS NORDION, INC.·Product code KXK·March 6, 2001

    THERASPHERE 20 GBQ

    FDA Adverse Event
    Injury ·MDS NORDION, INC.·Product code KXK·March 6, 2001

    THERASPHERE 20 GBQ

    FDA Adverse Event
    Injury ·MDS NORDION, INC.·Product code KXK·March 6, 2001