BEUDAMED
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    MODIFICATION TO THE MAESTRO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Safco Royal 4-ply bibs

    FDA UDI
    SAFCO DENTAL SUPPLY CO.·D72310201333·Safco Royal bib 13x18 4ply bge 500cs

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717101786·Burs FG 37, Pkg/100

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450046562·

    DRACO

    FDA UDI
    HNM TOTAL RECON LLC·00841742121833·DRACO MetaFuse BLP Plate, Ti - (L)33mm, L

    MENICON Z

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    NIR BILLIARY STENT SYSTEM; MARSHAL BALLOON DILATATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Widex

    FDA UDI
    Widex A/S·05706069718560·Widex EVOKE E-FA 330 DEMO (Silver Grey ) Teleco...

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC.·Product code LFR·May 25, 2007

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code FNL·March 25, 2013

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code HDD·March 10, 2011

    PERITONEAL CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·July 13, 2022

    PERITONEAL CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·December 8, 2022

    CSF-CARDIAC/PERITONEAL CATHETER, SMALL, 90CM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·December 8, 2022

    PERITONEAL CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·December 8, 2022

    PERITONEAL CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·December 8, 2022

    VUELOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    VEULOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    VEULOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020

    VEULOCK SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020