BEUDAMED
    32 results · 40ms · 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.

    ANSPACH KNOTLESS ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690124467·Modular Offset Stem 15mm x 75mm x 2mm

    MEDTRONIC PS MEDICAL CHANNELSCOPE ENDOSCOPE, MODELS 2232-001, 2232-002, 2232-003, 2232-004, 2233-002, 2233-005

    FDA 510(k)
    FDA Class 2 ·Neurology

    SOFT TISSUE SCREW AND WASHER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    G2 FILTER SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·August 21, 2007

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·March 25, 2015

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    LOCKING CAP

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code EZW·January 4, 2012

    G2 FILTER SYSTEM

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·May 15, 2007

    LIVIAN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 11, 2013

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·April 8, 2011

    BRAVO

    FDA Adverse Event
    Malfunction ·ARIZONA DEVICE MANUFACTURING·Product code FFT·May 22, 2008

    RECOVERY G2 FILTER SYSTEM - JUGULAR DELIVERY KIT

    FDA Adverse Event
    Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·March 23, 2010

    CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·December 29, 2015

    CLICKX PEDICSCR Ø6.2 L50 TAN DBLUE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013

    CLICKX-3D-HEAD F/PEDICSCR POST-OPEN TAN

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·February 12, 2013