BEUDAMED
    16 results · 20ms · Sources: EU EUDAMED, US FDA

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    VERSA-FX FEMORAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERSA-FXII SC TUBE PLT 90DX16H, 95DX16H, 95DX18H, 95DX20H, 95DX22H

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·June 21, 2017

    VERSA-FX II STD TUBE 130DX16H, 130DX18H, 130DX20H, 135DX16H, 135DX18H, 135DX20H, 140DX16H, 140DX18H, 140DX20H, 145DX16H, 145DX18H, 145DX20H, 150DX16H, 150DX18H, 150DX20H

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·June 21, 2017

    DURAFILL FLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    GL590 DIAGNOSTIC ULTRASOUND EQUIPMENT

    FDA 510(k)
    FDA Class 2 ·Radiology

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 5, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 5, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    BAERVELDT SHUNT

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code KYF·September 4, 2012

    TBD

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 11, 2013

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 10, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 24, 2014