BEUDAMED
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    Amvex Vacuum Regulator

    FDA UDI
    OHIO MEDICAL, LLC·00628101502119·VR-LP series, VacReg, Ped Int 3Mode 200mmHg, An...

    ADVANTX LC/LPN+

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS EUROPE·Product code IZI·August 23, 2001

    NOVA PLUS - PF EXAM GLV TEXTUR

    FDA Adverse Event
    Other ·ALLEGIANCE HEALTHCARE CORP·Product code LYY·March 9, 2001

    3CC SAF. SYR 20X1-1/2

    FDA Adverse Event
    Other ·KENDALL HEALTHCARE PRODUCTS·Product code MEG·March 1, 2001

    NOVA PLUS - PF EXAM GLV TEXTUR

    FDA Adverse Event
    Other ·ALLEGIANCE HEALTHCARE CORPORATION·Product code LYY·March 9, 2001

    HOMECHOICE AUTOMATED PD SET W/CASSETTE 4-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·May 20, 2003

    DENTIPS

    FDA Adverse Event
    Death ·MEDLINE·Product code KXF·December 11, 2008

    LIBERTY SELECT CYCLER ASSY(NON-VALUATED)

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code FKX·September 8, 2023

    HOYER LIFT

    FDA Adverse Event
    Injury ·TED HOYER AND CO., INC.·Product code FSA·September 30, 1994

    LIBERTY CYCLER SET, SINGLE PATIENT CONN

    FDA Adverse Event
    Malfunction ·ERIKA DE REYNOSA, S.A. DE C.V.·Product code FKX·September 8, 2023

    SAFTYGLIDE HYPODERMIC NEEDLE 25 GAUGE 1"

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY·Product code FMI·August 9, 2023

    READYMED

    FDA Adverse Event
    Malfunction ·MCGAW, INC.·Product code MEB·July 15, 1994

    ALENTI

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·March 10, 2011

    ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GCJ·April 4, 2022

    CLAVE NEEDLELESS CONNECTOR

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·May 25, 2000

    PREMIER NITROSPRAY REGULAR PLUS 16 OZ.

    FDA Adverse Event
    Injury ·PREMIER MEDICAL (MFG)·Product code GEH·March 26, 2004

    ALTADYNE

    FDA Adverse Event
    Death ·LUMEX·Product code FNM·December 10, 1997

    SHARPS CONTAINER DISPOSABLE

    FDA Adverse Event
    Malfunction ·SAGE PRODUCTS, INC.·Product code KPE·September 22, 1992

    PH HANDLE FOR YANK SUCT DEVICE

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code JOL·August 4, 2003

    VAIL

    FDA Adverse Event
    Injury ·VAIL PRODUCTS, INC.·Product code FNL·November 27, 1996