BEUDAMED
    35 results · 23ms · Sources: EU EUDAMED, US FDA

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    IS 40 MICROMOTOR

    FDA 510(k)
    FDA Class 1 ·Dental

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809870329·FOR MEN 30-40 MM HG THIGH MICRO DOT BAND CLOSED...

    VAPORIZED HYDROGEN PEROXIDE (VHP) STERILIZATION OF UHMWPE COMPONENTS IN THE REFLECTION ACTABULAR SYSTEM (ACETABULAR LINE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODEL 120, OXYSOFT, INFRARED DATA CONVERTER, MODEL 120

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY, INC.·Product code LFL·December 12, 2005

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·January 12, 2012

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code KWQ·October 30, 2009

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·July 3, 2019

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·Product code KWP·July 29, 2011

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·September 11, 2018

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·August 17, 2020

    VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 71/75 X 14MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 13, 2019

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·October 11, 2019

    VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 71/75X14MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·July 10, 2019

    5.0CM SHORT ATTACHMENT

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·April 2, 2013

    ENDOTAK RELIANCE G

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    KNEE IMPLANT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. ORTHOPAEDIC DIVISION·Product code JWH·April 7, 2011

    VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 63/67X14MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016