BEUDAMED
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    FLEXI-STAT SP02 EAR SENSOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JOBST forMen

    FDA UDI
    BSN MEDICAL, INC.·04042809867596·FOR MEN 30-40 MM HG THIGH MICRO DOT BAND OPEN T...

    MILLENNIUM EDITION 2000 ACCELERATED ELECTROFORMING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    REPROCESSED USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD PHOENIX¿ SMIC-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026

    BD VACUTAINER® BLOOD TRANSFER DEVICE WITH LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·November 29, 2017

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 28, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 14, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·May 27, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 20, 2026

    LOW PROFILE SELF-TAPPING BONE SCREW 6.5 MM X 25 MM

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LPH·April 6, 2011

    HARMONIC ACE SHEARS, 5.5 DIA, ERG HANDLE, CURVED

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, INC·Product code LFL·April 3, 2013

    ENDOTAK RELIANCE G

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

    BD PHOENIX¿ SMIC/ID-101

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 1, 2026

    ActiveLife One-Piece Drainable Pouch with Stomahesive Skin Barrier; 1 1/4 in., 32mm; Made in Dominican Republic; ConvaTec. Colostomy pouch

    FDA Recall
    Terminated ·Convatec Inc.·Product code EZQ·September 17, 2010

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025

    BD PHOENIX PANEL NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 2, 2025