BEUDAMED
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    HYPER AiR

    FDA 510(k)
    FDA Class 2 ·Radiology

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180171992·DOYEN RETRACTOR, BLADE SIZE 55MM X 35MM, 9-1/2"

    PBC Separator with Selux AST System

    FDA UDI
    Selux Diagnostics, Inc.·00850031114067·

    4.0mm/2.5mm Drill Sleeve

    FDA UDI
    Osteocentric Technologies, Inc.·00810074300865·4.0mm/2.5mm Drill Sleeve

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989044065·CROWN-PERM UL 1 MOLAR SST PK/5

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481124341·LOCATOR R-Tx Attachment System for 3.5 Internal...

    Bard Stinger Ablation Catheter: Item Numbers 210001 218501 L210001 210002 218502 L210002 210003 218503 L210003 210004 218504 L210004 210005 218505 L210005 210006 218506 L210006 210007 218507 L210007 210015 218516 L210008 210016 218518 L210009 210017 218519 L210010 210018 218520 L210011 210019 218521 L210012 210020 218523 L210013 210023 218524 L210014 210024 218525 L210015 210025 218526 L210016 210026 218527 L210017 210027 218528 L210018 210028 218529 210029 210030

    FDA Recall
    Terminated ·C. R.Bard, Inc./Electrophysiology Division·January 8, 2003

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946071653·X SERIES, HOSPITAL, MONITOR/DEFIBRILLATOR, NELL...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946059729·X SERIES, MONITOR/DEFIBRILLATOR, NELLCOR, 3/5 L...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946018580·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946099497·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376301419·Silicone Handle, Ball, Large 1/4" QC Modular, I...

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376301334·Silicone Handle, Egg, Medium 1/4" QC Modular, I...

    Universal Dilator

    FDA UDI
    SPINEOLOGY INC.·M7405210001·Pedicle Marker Inserter

    Control Unit Battery

    FDA UDI
    Scibase AB·07350094440194·Battery used in addition to the power cord for ...

    LIVESURE THC SCREEN TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SPACELABS PATHFINDER SL HOLTER ANALYZER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Immunohistochemistry Test, Dna Mismatch Repair (Mmr) Protein Assay

    FDA Pre-Market Approval
    FDA Class 3 ·VENTANA MMR RxDx Panel

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523171965·Tribrid Femoral Trials Instrument Case Base

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523171972·Tribrid Femoral Trials Instrument Case Tray