BEUDAMED
    39 results · 21ms · Sources: EU EUDAMED, US FDA

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    INTELLISPHERE EVENT MANAGMENT SYSTEM REL. 10.00

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AUTION™ MAX AX-4022 Analyzer

    FDA UDI
    ARKRAY USA, INC.·00015482129743·Urine Analyzer utilize reflectance technology w...

    Recon

    FDA UDI
    Revelation Medical Devices·G3181029740·Narrow Glenoid Retractor

    EMIT TOX ACETAMINOPHEN ASSAY, MODEL 7A319UL; EMIT TOX ECETAMINOPHEN CALIBRATORS, MODEL 7A409UL

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    PRIZM MEDICAL INC. THERMOTRACE INFRARED THERMOMETER MODELS 15004 AND 15007

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·December 4, 2012

    LIFEPAK® 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·February 6, 2019

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·September 24, 2015

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 19, 2014

    INTEGRITY RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MAF·May 12, 2011

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·October 25, 2019

    SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

    FDA Adverse Event
    Injury ·COOK INC·Product code FOZ·April 2, 2019

    SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·March 14, 2018

    LJS TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·May 11, 2018

    SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·February 15, 2018

    SPECTRUM TURBO-JECT ANTIBIOTIC POWER INJECTABLE PICC

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·February 15, 2018

    LJS TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·May 11, 2018