BEUDAMED
    53 results · 21ms · Sources: EU EUDAMED, US FDA

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    PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1020400·10mm H x 20mm W x 40mm L x 0 degrees XLIF

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741020400·

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540134288·ORBITAL RIM RETRACTOR

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR21020401·Compound retraction arch max. .016"x.022" / 45°

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X102040120·10mm H x 20mm W x 40mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L102040120·10mm H x 20mm W x 40mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X10204080·10mm H x 20mm W x 40mm L x 8 degrees XLIF

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR21020400051·Compound retraction arch max. .016"x.022" / 45°

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674102040060·

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR21020400101·Compound retraction arch max. .016"x.022" / 45°

    Viceroy

    FDA UDI
    DIOMEDICAL CO.,LTD.·08800039825849·Rod 5.5 x 40mm

    FMS SOLO

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RAMP MYOGLOBIN ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    SMARTSETMV MV ENDURANCE 40 G

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 3015516266·Product code MBB·June 13, 2025

    AQUILEX FLUID CONTROL SYSTEM

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·March 12, 2020

    Bemis Two-Gallon Sharps Container, Models #102 020, #102 030, and #102 040. (The only difference between the models is in color. Model 102 040 is yellow, Model 102 020 is beige and Model 102 030 is red. )

    FDA Recall
    Terminated ·Product code MMK·February 25, 2004

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 22, 2013

    ARCHITECT CA 125 II

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LTK·August 7, 2008