BEUDAMED
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    BACTI PLATE (DERMATOLOGY) PRODUCT NO. PS-5000

    FDA 510(k)
    FDA Class 2 ·Microbiology

    REGO HUB,HILLROM NAVICARE,NO-NC,NO-P

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828192668·REGO HUB,HILLROM NAVICARE,NO-NC,NO-P

    REGO HUB,ASCOM TELLIGENCE,NO-NC,NO-P

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828192699·REGO HUB,ASCOM TELLIGENCE,NO-NC,NO-P

    NOP-P ANAESTHESIA MASK#5 ,DISPOSABLE,A TYPE-BLUE

    FDA UDI
    BESMED HEALTH BUSINESS CORP.·04716770657516·NOP-P ANAESTHESIA MASK#5 ,DISPOSABLE,A TYPE-BLUE

    REGO HUB,HILLROM NAVICARE,NO-NC,NO-P,ALT

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828192682·REGO HUB,HILLROM NAVICARE,NO-NC,NO-P,ALT

    CAPSURE FIX MRI

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·February 7, 2022

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·April 11, 2014

    VITALITY AVT

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·November 9, 2004

    INGEVITY+

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NVN·April 12, 2024

    CYLOS DR-T

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH AND CO·Product code DXY·October 25, 2007

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·November 14, 2005

    MX40 1.4 GHZ SMART HOPPING

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DSI·June 11, 2019

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 14, 2013

    IN TOUCH EU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 15, 2011

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·July 9, 2009

    *

    FDA Adverse Event
    Injury ·MEDTRONIC MILACA INC.·Product code DTE·September 10, 1998

    INTELLIVUE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·March 16, 2020

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 8, 2018

    WEST NILE VIRUS ASSAY

    FDA Adverse Event
    Injury ·NOT IDENTIFIED·Product code NOP·February 6, 2007

    WEST NILE IGM EIA

    FDA Adverse Event
    Injury ·FOCUS DIAFNOSTICS·Product code NOP·October 10, 2014