BEUDAMED
    954 results · 25ms · 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 ×

    ULTRA-DRIVE DISK DRILL

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code LZV·May 6, 1999

    CONCISE CEMENT SCULPS KIT

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW RICHARDS, INC.·Product code LZV·February 3, 1995

    ULTRA - DRIVE DISK DRILL

    FDA Adverse Event
    Other ·BIOMET, INC.·Product code LZV·January 12, 2007

    *

    FDA Adverse Event
    Other ·BIOMET, INC.·Product code LZV·June 2, 1997

    ULTRA-DRIVE PLUG PULLER

    FDA Adverse Event
    Injury ·*·Product code LZV·June 2, 1997

    GRAY REVISION CEMENT FORCEPS

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code LZV·October 2, 1996

    GRAY REVISION CEMENT FORCEPS

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code LZV·December 6, 1996

    EXETER INTRODUCER EXTRACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC·Product code LZV·October 21, 1996

    OSCAR

    FDA Adverse Event
    Malfunction ·ORTHOFIX SRL·Product code LZV·October 31, 2018

    OSCAR 3

    FDA Adverse Event
    Malfunction ·ORTHOFIX INC.·Product code LZV·January 20, 2017

    RENOVATION

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV·Product code LZV·November 13, 2006

    BIOMET 9.5 MM DISK DRILL TIP

    FDA Adverse Event
    Other ·BIOMET. INC.·Product code LZV·December 5, 2006

    ULTRA-DRIVE DISK DRILL

    FDA Adverse Event
    Injury ·ARTHROTEK/BIOMET·Product code LZV·May 20, 2004

    ULTRA-DRIVE DISK DRILL

    FDA Adverse Event
    Injury ·ARTHROTEK/BIOMET·Product code LZV·May 2, 2003

    ULTRA DRIVE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZV·July 20, 2007

    ULTRA - DRIVE DISK DRILL

    FDA Adverse Event
    Other ·BIOMET, INC.·Product code LZV·February 23, 2005

    SMITH NEPHEW RICHARD

    FDA Adverse Event
    Malfunction ·SMITH NEPHEW RICHARD·Product code LZV·March 9, 2005

    INTERCONDYLAR FEMORAL CHISEL

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LZV·May 1, 2008

    MORELAND CEMENT REMOVAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LZV·December 27, 2004

    ULTRA-DRIVE DISK DRILL

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code LZV·August 9, 1999