BEUDAMED
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    FRW-01

    FDA UDI
    MCT Bio·08800021124097·Remover Wrench BONE-EXPANDER-WRENCH

    Neobiotech Implant System

    FDA UDI
    Neobiotech. co., ltd·08800263100132·N&R/W Type

    DRILL CONICAL Ø4.5MM

    FDA UDI
    Sin Sistema de Implante Nacional S/A·07899995208828·DRILL CONICAL Ø4.5MM

    DRILL CONICAL Ø5.5MM

    FDA UDI
    Sin Sistema de Implante Nacional S/A·07899995208835·DRILL CONICAL Ø5.5MM

    DRILL CONICAL Ø4.1MM

    FDA UDI
    Sin Sistema de Implante Nacional S/A·07899995296184·DRILL CONICAL Ø4.1MM

    DRILL CONICAL Ø3.8MM

    FDA UDI
    Sin Sistema de Implante Nacional S/A·07899995208811·DRILL CONICAL Ø3.8MM

    CAPSUREFIX LEAD

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 15, 2019

    PERCOR STAT-DL 9.5 FR W/OPT INSERT W/O INTRO SHEAT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SURESTEP¿ FOLEY TRAY SYSTEM BARDEX® ALL- SILICONE FOLEY CATHETER TRAY

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC.·Product code EZL·April 28, 2025

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·May 21, 2025

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·May 21, 2025

    CAPSURE FIX MRI

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO VILLALBA·Product code NVN·September 15, 2025

    CAPSURE FIX MRI

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO VILLALBA·Product code NVN·September 15, 2025

    CAPSUREFIX NOVUS LEAD MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·April 22, 2025

    CAPSUREFIX NOVUS LEAD MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·April 22, 2025

    8.0 FR W/VITACUFF

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD)·Product code LJS·October 29, 2007

    BROV 4.2 FR W/VITA

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BASD)·Product code DQO·February 5, 2007

    8.0 FR W/-4 VITACUFF PERC

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS·Product code LJS·November 28, 2018

    204 BROV 4.2 FR W/VITACUFF

    FDA Adverse Event
    Injury ·3600-C.R. BARD ACCESS SYSTEMS PRODUCTS·Product code DQO·March 1, 2001

    204 BROV 4.2 FR W/VITAC

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (PUERTO RICO)·Product code DQO·August 15, 2001