BEUDAMED
    172 results · 28ms · Sources: EU EUDAMED, US FDA

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    M.R. ASSOC. WASHING TUBE/MEASURING TUBE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LITE WAND II

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PICO SMOKERLYZER, MODEL EC-50

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·May 8, 2014

    UNKNOWN ZIMMER KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·October 18, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 7, 2007

    DRILL

    FDA Adverse Event
    Malfunction ·MEDTRONIC (1-800-962-9888)·Product code HBE·March 30, 2016

    ENDO CATCH II 15 MM

    FDA Adverse Event
    Injury ·COVIDEN (DISTRIBUTED BY CARDINAL HEALTH 1-800-964-5227) 1-800-962-9888·Product code GCI·August 12, 2015

    Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000

    FDA Recall
    Open, Classified ·Covidien·Product code CCW·September 28, 2023

    Cardio Medical Products, Inc. Defibrillation/Cardioversion/Monophasic or Biphasic Pacing/ECG Electrode Rx Only Single Patient Use Only Manufactured for Cardio Medical Products 385 Franklin Avenue, Suite L Rockaway, New Jersey 07866 www.cardiomedicalproducts.com (800) 227-3633 (973) 586-9624 FAX Defibrillator

    FDA Recall
    Terminated ·Cardio Medical Products·Product code LDD·April 26, 2013

    Patient-Fitted Temporomandibular (TMJ) Reconstruction Prosthesis

    FDA Recall
    Open, Classified ·Stryker Leibinger GmbH & Co. KG Botzinger Str. 41 Freiburg Im Breisgau Germany·Product code LZD·December 6, 2022

    Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.

    FDA Recall
    Terminated ·Covidien LLC·Product code DRO·April 8, 2013

    Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles

    FDA Recall
    Terminated ·Covidien LLC·Product code LRO·September 29, 2016

    Covidien Devon Light Glove packaged in sterile surgical kits Reference: 31140208 Product Usage: A disposable, sterile, single-use cover for compatible surgical light handles

    FDA Recall
    Terminated ·Covidien LLC·Product code LRO·September 29, 2016

    Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode Product ID: 22550P. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.

    FDA Recall
    Terminated ·Covidien LLC·Product code DRO·April 8, 2013

    Step Bladeless Trocars, 10 mm cannula and dilator with radially expandable sleeve and 5 - 10 mm reducer, Product Number S101010

    FDA Recall
    Open, Classified ·Product code GCJ·March 1, 2023

    Mild Chromic Gut Absorbable Sutures, CH GUT 5-0 12 UD SS-14 SS-14 (G-1766-K), CHROMIC GUT 6-0 45CM HE-1 X12 (G-1780K)

    FDA Recall
    Open, Classified ·Product code GAL·March 1, 2023

    Plain Gut Absorbable Sutures, PLAIN GUT 5/0 18 P-13 X12 (SG-5686), PLAIN GUT 4-0 18 UD SC-11 DA (SG828-2)

    FDA Recall
    Open, Classified ·Product code GAL·March 1, 2023

    MEDPOR PLUS SST EZ 22mm Sphere Implant, Howmedica Osteonics Corp, 15 Dart Road, Newnan, GA 30265. MEDPOR PLUS Orbital Implants are intended to restore the volume of an enucleated or eviscerated eye globe.

    FDA Recall
    Terminated ·Howmedica Osteonics Corp dba Stryker Craniomaxillofacial·Product code HPZ·March 20, 2012

    QUINTUBE Monitor Pack (5 tubes/pk, 24 pk/case) (Non-Sterile) SPG Bulb Drain System, 4mm Flat w/Center Holes (Sterile) Accessories to TLS Surgical Drainage System

    FDA Recall
    Terminated ·Stryker Leibinger GmbH & Co. KG Botzinger Strasse 41 Freiburg Germany·Product code GCY·January 3, 2017