BEUDAMED
    52 results · 20ms · Sources: EU EUDAMED, US FDA

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    ARGYLE RIGID URINE MEASURING/COLL. DEV.

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

    NUPRO® Sensodyne® Prophylaxis Paste with Fluoride and NovaMin®

    FDA UDI
    DENTSPLY INTERNATIONAL INC.·D0038015221·NUPRO® Sensodyne® Prophy Paste, Orange, Polish,...

    Acumed

    FDA UDI
    Provision·B504OM8015220·

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776354091·Malis Scissor

    ACUMED

    FDA UDI
    Acumed LLC·10806378049460·Micro Acutrak 2® Extended Long Drill

    Symmetry Verity™

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482030981·Verity Scissors, Bayonet, Straight, Regular Tip...

    ACTIVA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·January 6, 2012

    Curette

    FDA UDI
    BICON, LLC·00813110025814·Lucas Bone Curette

    TRANSQ3

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BIO NUCLEAR DIAGNOSTICS (ENDO)CERVICAL SAMPLER FOR GYN CYTOLOGY

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ACTIVA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·February 7, 2013

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 9, 2014

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·October 16, 2007

    HI-TORQUE PROGRESS 80 GUIDE WIRE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code DQX·October 23, 2012

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 14, 2012

    Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00219W, 24F x 4.4cm, 20cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116. A silicone low-profile balloon-type device is designed for percutaneous insertion through an established, appropriately sized stoma tract. It is a component of the Dual Port Wizard Gastrostomy Device.

    FDA Recall
    Terminated ·C R Bard Inc·Product code KNT·December 22, 2008

    Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00201W, 16F x 1.7cm, 10cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116. A silicone low-profile balloon-type device is designed for percutaneous insertion through an established, appropriately sized stoma tract. It is a component of the Dual Port Wizard Gastrostomy Device.

    FDA Recall
    Terminated ·C R Bard Inc·Product code KNT·December 22, 2008

    Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00221W, 18F x 1.2cm, 10cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116. A silicone low-profile balloon-type device is designed for percutaneous insertion through an established, appropriately sized stoma tract. It is a component of the Dual Port Wizard Gastrostomy Device.

    FDA Recall
    Terminated ·C R Bard Inc·Product code KNT·December 22, 2008

    Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00218W, 24F x 3.4cm, 20cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116. A silicone low-profile balloon-type device is designed for percutaneous insertion through an established, appropriately sized stoma tract. It is a component of the Dual Port Wizard Gastrostomy Device.

    FDA Recall
    Terminated ·C R Bard Inc·Product code KNT·December 22, 2008

    Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00214W, 20F x 3.4cm, 20cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116. A silicone low-profile balloon-type device is designed for percutaneous insertion through an established, appropriately sized stoma tract. It is a component of the Dual Port Wizard Gastrostomy Device.

    FDA Recall
    Terminated ·C R Bard Inc·Product code KNT·December 22, 2008