BEUDAMED
    14 results · 36ms · Sources: EU EUDAMED, US FDA

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    SYNTEC-TAICHUNG NON-STERILE BONE PLATE AND SCREW IMPLANTS, MODEL#'S 222020-248120, 240050-240980, 241130-246620, 4240420

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BILOX PROSTHESIS HEAD 12/14 28MM L

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

    MEDIUM 199, 10X, CATALOG NO. 210-3555

    FDA 510(k)
    FDA Class 1 ·Hematology

    MODIFICATION TO: METHA HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

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

    BIOLOX PROSTHESIS HEAD 12/14 32MM L

    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 AND CO. KG·Product code LWJ·March 6, 2014

    PRIMEADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·February 28, 2013

    TRANSITIONLESS MICROPUNCTURE INTRODUCER SET, STAINLESS STEEL

    FDA Adverse Event
    COOK·Product code DQX·January 21, 2011

    ALAIR?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code OOY·August 6, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·April 14, 2015

    Philips Azurion system; Software Version Number: R3.1;

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·January 28, 2026