BEUDAMED
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    INTRICON DATRIX CENTAURI MT AMBULATORY PATIENT ECG TELEMETRY SYSTEM (APETS)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169601437·SPACER 2111160 OLIF25 20MM 6 DEG 8X60

    NA

    FDA UDI
    MAKO SURGICAL CORP.·00848486002763·SQUARE DRIVER

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540138972·CONDYLAR NECK RETRACTOR,SALZBURG,LEFT

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08806390850049·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197257053·ATRAUMA Babcock Intestinal Forceps 160mm,...

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089402793·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197030038·Metzenbaum scissors, Fig.1 curved 16cm, ...

    E-Z EM PERCUPUMP 2001 CT INJECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    ROCHE ORAL FLUID COCAINE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Pharmaceutical Innovations

    FDA UDI
    PHARMACEUTICAL INNOVATIONS INC·00300361111606·Other-Sonic High Viscosity Generic Ultrasound G...

    POWERFLEX P3 PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code LIT·May 14, 2013

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 23, 2014

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD/HUNTINGTON·Product code MFK·May 26, 2011

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 13, 2024

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

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

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

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