BEUDAMED
    18 results · 29ms · 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.

    Epiduroscopy Introducer Set

    FDA UDI
    MYELOTEC, INC.·M79340075·

    Video Guided Catheter

    FDA UDI
    MYELOTEC, INC.·M79320105·3.0 Video Guided Catheter

    Video Guided Catheter

    FDA UDI
    MYELOTEC, INC.·M79320335·Video Guided Catheter

    Epiduroscopy Introducer Set

    FDA UDI
    MYELOTEC, INC.·M79340085·Epiduroscopy Introducer Set

    NaviCath

    FDA UDI
    MYELOTEC, INC.·M79320175·NaviCath Steerable Catheter Kit

    VIDEO GUIDED CATHETER

    FDA Adverse Event
    Other ·MYELOTEC, INC.·Product code HRX·February 15, 2011

    ARTHROSCOPE

    FDA Adverse Event
    Injury ·MYELOTEC, INC.·Product code HRX·October 31, 2014

    VIDEO GUIDED CATHETER

    FDA Adverse Event
    Injury ·MYELOTEC, INC.·Product code HRX·December 7, 2012

    2017 NAVICATH KIT

    FDA Adverse Event
    Injury ·MYELOTEC, INC.·Product code HRX·December 30, 2013

    MYELOTEC SPINAL ENDOSCOPY ACCESS KIT

    FDA Adverse Event
    Malfunction ·MYELOTEC, INC.·Product code HRX·June 11, 2013

    UNK

    FDA Adverse Event
    Injury ·MYELOTEC, INC.·Product code HRX·July 11, 2012

    2010 VIDEO GUIDED CATHETER

    FDA Adverse Event
    Malfunction ·MYELOTEC, INC·Product code HRX·April 13, 2017

    2017 NAVICATH KIT

    FDA Adverse Event
    Malfunction ·MYELOTEC, INC·Product code HRX·April 13, 2017

    MYELOTEC NAVICATH STEERABLE EPIDURAL CATHETER

    FDA Adverse Event
    Other ·MYELOTEC, INC.·Product code BSO·January 11, 2008

    Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels

    FDA Enforcement
    Class II ·Ongoing·Myelotec, Inc.·August 9, 2017

    Myelotec Steerable Video Guided Catheter, 3.0mm, Label Insert contained in LB0020-0, LB0020-1, LB0020-2, LB0020-3, and LB0020-4 (Product Code: 2010). Myelotech, Roswell, GA 30076.

    FDA Recall
    Terminated ·Myelotec, Inc.·Product code HRX·December 19, 2007

    Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels

    FDA Recall
    Open, Classified ·Myelotec, Inc.·Product code HRX·March 2, 2017

    Myelotec Steerable Video Guided Catheter, 2.7mm, label insert for LB0013-1, LB0013-2, and LB0013-3. (product code: 2000) Myelotech, Roswell, GA 30076.

    FDA Recall
    Terminated ·Myelotec, Inc.·Product code HRX·December 19, 2007