BEUDAMED
    12 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    WAND PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    REMEL SPECTRA VRE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    OEC Elite

    FDA 510(k)
    FDA Class 2 ·Radiology

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATIA)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·June 7, 2006

    NOTINGHM SHLDR HUM HEAD 48X17 OFFSET

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWS·January 19, 2016

    BEACON TIP ROYAL FLUSH PLUS FLUSH CATHETER

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DQO·February 27, 2013

    7600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 4, 2011

    SECURA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020

    GORE® DUALMESH® BIOMATERIAL

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTL·November 12, 2020