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

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    SYNERGY CEMENTED HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRODRIVE LINE OF DENTAL HANDPIECES

    FDA 510(k)
    FDA Class 1 ·Dental

    M-Y Sheath

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEO·June 19, 2006

    UNKNOWN ACETABULAR HIP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·March 5, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 7, 2014

    EMBRYO RPLCMNT CATHETER

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code MQF·September 24, 2019