BEUDAMED
    22 results · 21ms · Sources: EU EUDAMED, US FDA

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    NobelSpeedy Groovy

    FDA 510(k)
    FDA Class 2 ·Dental

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694004374·LOGIC Distractor, Right Straight

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694031226·.035 x 4 Double Trocar K-wire

    B-P TOTAL HIP SYSTEM

    FDA UDI
    ENDOTEC, INC.·00814193023902·B-P MODULAR EXTENSION W/ULTRACOAT - 19 MM X 25 MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694068048·.035" x 4" Double Trocar K-wire Sterile Qty 5

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·February 7, 2017

    MCKINLEY SATURATION CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PRESSURE MANOMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Widex

    FDA UDI
    Widex A/S·05706069923773·WIDEX MOMENT MBB3D 50 (Silver grey)

    Widex

    FDA UDI
    Widex A/S·05706069895964·WIDEX EVOKE E-FA (Silver Grey ) 50, Telecoil, V...

    Widex

    FDA UDI
    Widex A/S·05706069870688·WIDEX EVOKE E-FM (Silver Grey ) 50, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069897623·WIDEX EVOKE E-FP (Silver Grey ) 50, Telecoil, V...

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·October 10, 2014

    SOFTCLIX ® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·June 10, 2013

    LANDMARX EVOLUTION

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC.·Product code HAW·May 13, 2011

    INFANT DUAL HEATED EVAQUA2 BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·July 11, 2016

    .035 X 4" DOUBLE TROCAR K-WIRE

    FDA Adverse Event
    Injury ·OSTEOMED·Product code HWC·January 18, 2019

    SPEED TITAN 15X15X15MM IMPLANT, INSERTER

    FDA Adverse Event
    Malfunction ·BIO MEDICAL ENTERPRISES INC·Product code JDR·September 12, 2016

    Artis zeego, Model Number 10280959

    FDA Enforcement
    Class II ·Terminated·Siemens Medical Solutions USA, Inc·July 31, 2019

    Artis zeego, Model Number 10280959

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc·April 27, 2022