BEUDAMED
    44 results · 26ms · Sources: EU EUDAMED, US FDA

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    EsophyX2 HD Device with SerosaFuse Fasteners and Accessories, EsophyX Z Device with SerosaFuse Fasteners and Accessories

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

    ESOPHYX Z

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293326·

    NA

    FDA UDI
    KEY SURGICAL, INC.·10849771049538·K-Wires, Single diamond threaded, .062-inch (1....

    INTEGRAL X-SERIES HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304650367·

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383552509·Gutta Percha Points is used to root canal filin...

    InFill Lordotic ACF

    FDA UDI
    PINNACLE SPINE GROUP, LLC·00814729025561·

    InFill Anatomic ACF

    FDA UDI
    PINNACLE SPINE GROUP, LLC·00814729025684·

    BLOOD GLUCOSE MONITORING SYSTEM, MODELS AG-6081 AND AG-6951

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENTUIT GASTROSTOMY BR BALLOON RETENTION FEEDING TUBE WITH ENFIT CONNECTION

    FDA Adverse Event
    Injury ·XERIDIEM MEDICAL DEVICES·Product code PIF·April 18, 2018

    TRI TS BASEPLATE SIZE 3

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·July 15, 2011

    ESPRIT VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·October 14, 2014

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·September 22, 2008

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019

    VITALITY SCREW, UNKNOWN SIZE OR TYPE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019