BEUDAMED
    22 results · 28ms · Sources: EU EUDAMED, US FDA

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    GLOBAL(TM) TOTAL SHOULDER W/DUPONT ENHANCED UHMWPE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERTE-SPAN® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·20721902068342·M4 BREAK-OFF SCREW

    Hammer

    FDA UDI
    ADLER ORTHO SPA·08050507138081·REINFORCED GENUS MODULAR SLAP HAMMER ASSEMBLY

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450749913·

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0140000·Counter Torque, Offset Handle Assembly

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K0140000·Counter Torque, Standard and Extended Tab

    VISTITOME 20-10 MICROKERATOME

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    TROJAN(R) EXTRA STR LATEX CONDOM W/SPERM SILI LUBR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 14, 2013

    POSEY SITTER SELECT

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·November 19, 2010

    MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT

    FDA Adverse Event
    C.T.M. TAIWAN·Product code INI·July 3, 2014

    BD PrepStain System, Model Number: 799-14000-00; Catalog Number: 05CR000021, 05CR00021R, 799-13000-00, 799-13000-00R, 799-14000-00 and 799-14000-00R; Catalog Number: 05CR000021, 05CR000021R, 799-13000-00, 799-13000-00R, 799-14000-00 and 7914000-00R. PrepStain is a liquid-based thin layer cell preparation device for preparation and staining of Prep smear slides from cervical specimens in a liquid based format (gyn use) and of cytology examination slides from non-cervical specimens such as urine and lung lavage.

    FDA Recall
    Terminated ·Bd Diagnostic Systems Tripath·Product code MKQ·September 26, 2008