BEUDAMED
    9 results · 20ms · 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 ×

    1.5MM TI OBLIQUE L-PLATE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·September 9, 2003

    CABLE TENSIONER

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code LXH·December 10, 2014

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ+ TECHNOLOGY

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code QFG·November 26, 2025

    FLANGE FIXTURE AND ABUTMENT

    FDA Adverse Event
    Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 11, 2011

    INLAY FOR A STRATEC CUP, SIZE 50/28 DYSPLASIA.

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 2, 2018

    PROTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·SYNTHES(USA)·Product code MDI·March 9, 2015

    PROTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MDI·March 9, 2015

    CLARITY CONSOLE

    FDA Adverse Event
    Injury ·STRYKER ENDOSCOPY-SAN JOSE·Product code LLZ·January 7, 2019

    OT ULTRALINK METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2014