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

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    MAEDA NEW NEEDLE DISPOSABLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741110702·Catheter Placement Kit

    Preat

    FDA UDI
    Preat Corporation·00842092131350·NobelBiocare™ Tri-Lobe-compatible RP 17° Multi-...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092116579·NobelBiocare™ Tri-Lobe-compatible RP 17° Multi-...

    CUSTOM PROCEDURE KIT

    FDA UDI
    MEDIVATORS INC.·40677964004740·CUSTOM PROCEDURE KIT

    ER920W Cardiolabs

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WCL20·Wireless Arrhythmia Event Recorder

    ER920W CardioNet

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WCN0·Wireless Arrhythmia Event Recorder

    ER920W Brookings Health

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WBH0·Wireless Arrhythmia Event Recorder

    ER920W CardioLabs

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WCL0·Wireless Arrhythmia Event Recorder

    ER920W Empire Scanning

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WES0·Wireless Arrhythmia Event Recorder

    ER920W First-Call Medical

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WFCM0·Wireless Arrhythmia Event Recorder

    ER920W Life Support

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WLS0·Wireless Arrhythmia Event Recorder

    ER920W NCMC

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WNC0·Wireless Arrhythmia Event Recorder

    ER920W UNM

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146UNM0·Wireless Arrhythmia Event Recorder

    ER920W Cardiomedix

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WCM0·Wireless Arrhythmia Event Recorder

    ER920W Braemar

    FDA UDI
    BRAEMAR MANUFACTURING, LLC·B146ER9WB0·Wireless Arrhythmia Event Recorder

    MANUAL AND REMOTE CONTROLLED APPLICATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    HARDYDISK, CARBENICILLIN, 100MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·November 25, 2024

    MAQUET POWERLED II

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FTD·October 30, 2024