BEUDAMED
    33 results · 24ms · Sources: EU EUDAMED, US FDA

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    LAGUNA PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012

    803-050060-150

    Device
    EU MDR · Eu Md Class 2a ·BrosMed Medical Co., Ltd·On the market·32 countries

    NA

    FDA UDI
    Yeti Dentalprodukte GmbH·EYET6050060·Bite Registration Wax brown

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955934155·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955933547·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 35 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955932939·Percutaneous Transluminal Angioplasty Balloon C...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710410500600·Anterior Closing Wedge Osteotomy Guide, 50mm x ...

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420500600·Anterior Lateral Wedge Osteotomy Guide, 50mm x ...

    Mariner Outrigger

    FDA UDI
    Seaspine Orthopedics Corporation·10889981172923·L Con, Side-Loading, R, 8mm, 60mm

    PERSONA® Persona SoluTion™

    FDA UDI
    Zimmer, Inc.·00889024231313·

    PERSONA® Persona SoluTion™

    FDA UDI
    Zimmer, Inc.·00889024231320·

    GEL MARK BIOPSY SITE MARKER, MODELS MKOOO1, MK0004, MK0007

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

    RITA STARBURST XLI ELECTROSURGICAL DEVICE

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

    HISTOACRYL TISSUE ADHES.TRNS 0.5ML

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code MPN·February 23, 2016

    GORE PROPATEN VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·January 14, 2019

    LNOP MP12 PATIENT CABLE

    FDA Adverse Event
    Malfunction ·MASIMO CORPORATION·Product code DQA·May 15, 2015

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·GUIDANT PUERTO RICO BV·Product code NVY·April 10, 2013

    40 LTR HIGH FLOW INSUFFLATOR (W/POWER CORD & VERES

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCX·April 4, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·May 22, 2008