BEUDAMED
    52 results · 22ms · Sources: EU EUDAMED, US FDA

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    MI DeTACH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481124396·LOCATOR R-Tx Attachment System for 3.5 Internal...

    Zavation

    FDA UDI
    Zavation LLC·00842166132108·Ti3Z CIF 13mmx15mmx6mm -0 deg

    n/a

    FDA UDI
    Ortho Development Corporation·00822409078073·Acetab Trial Impactor Handle

    4.0 Super Fastener Screw Tap, 145mm

    FDA UDI
    Osteocentric Technologies, Inc.·00810074300872·4.0 Super Fastener Screw Tap, 145mm

    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

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376301464·Silicone Handle, Ball, Large 1/4" QC Modular, I...

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376301389·Silicone Handle, Egg, Medium 1/4" QC Modular, I...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540225987·BONE SCREWS, CROSS-FIT, SELF-TAPPING

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193114262·HA PEEK EVOS Straight, ,6mmx11mmx 26mm , FLAT ...

    MULTI-IMAGE CAMERA, SERIES 2100, MODEL #2100-06

    FDA 510(k)
    FDA Class 2 ·Radiology

    OIS SYMPHONY IMAGE MANAGMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    DRAINAGE CATHETER OR FOLEY CATHETER

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

    Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·Thoraflex™ Hybrid

    INFINION 16

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 2, 2023

    VENA SEAL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code PJQ·May 17, 2021

    CLOSUREFAST CATHETER

    FDA Adverse Event
    Injury ·COVIDIEN·Product code GEI·May 17, 2021

    PERSONA™

    FDA UDI
    Zimmer, Inc.·00889024239777·

    PERSONA®

    FDA UDI
    Zimmer, Inc.·00889024642157·

    PERSONA™

    FDA UDI
    Zimmer, Inc.·00889024239814·