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

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    SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX

    FDA 510(k)

    OnBrace Crown UR5 (5/pk)

    FDA UDI
    SPECIALTY APPLIANCES, LLC·D8199013210·

    NEEDLEHOLDER INSERT

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09929013210·NEEDLEHOLDER WITH TUNGSTEN CARBIDE SERRATED CRO...

    Mini Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746110207·DB BKT MINI MS LR 2ND BIC 018 T-22 A=0 R4D

    OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ALL-PRO 2010

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    ACUTRAK SCREW

    FDA Adverse Event
    Malfunction ·ACUMED LLC·Product code HWC·January 28, 2019

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 30, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 8, 2013

    SETROX S 53

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·November 9, 2010