BEUDAMED
    39 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ULTRACAPS S

    FDA 510(k)
    FDA Class 2 ·Dental

    SI ASCOPE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    STARION INSTRUMENTS POWER POINT CAUTERY CLAMP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BILOX PROSTHESIS HEAD 12/14 28MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·May 23, 2014

    EXCIA L PLASMAPORE UCAP 8/10 SIZE 11MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    ISODUR PROSTHESIS HEAD 12/14 32MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG&CO KG·Product code LPH·August 7, 2014

    QUINTEX SEMICONSTRAINED SCREW 4.0X16MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    EXCIA PLASMAPORE-UCAP 8/10 SIZE 11MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code MEH·June 21, 2013

    EXCIA CEMENTED 8/10 SIZE 12MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code JDI·November 5, 2012

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 14, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    IPC® STYLUS TRANSNASAL BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·February 6, 2015

    IPC® HANDPIECE - XPS® STRAIGHTSHOT® M4

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC·Product code ERL·June 19, 2015

    BIOLOX PROSTHESIS HEAD 12/14 32MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    XPS® BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·September 8, 2017

    BIOLOX PROSTHESIS HEAD 8/10 32MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LZO·June 21, 2013

    ACCY EF201 IPC FOOT CONTROL ROHS

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code HBE·September 9, 2014

    XPS® BUR - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code EQJ·June 17, 2016

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·April 26, 2013