BEUDAMED
    26 results · 24ms · Sources: EU EUDAMED, US FDA

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    MINI CANNULATED HEADED AND HEADLESS SCREW SET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Spherodon - M

    FDA UDI
    SILMET LTD·07290012207389·Dental Amalgam Capsules

    AED

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657017848·Wide Jaw Punch large 3.5mm 30 degree left

    BAXTER COLLEAGUE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code FRN·June 15, 2011

    TANDEMHEART PUMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNTEX POWDER-FREE NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NOVOSYN

    FDA Adverse Event
    Injury ·B. BRAUN SURGICAL, S.A.·Product code GAM·May 26, 2021

    NOVOSYN

    FDA Adverse Event
    Injury ·B. BRAUN SURGICAL, S.A.·Product code GAM·May 26, 2021

    NOVOSYN

    FDA Adverse Event
    Injury ·B. BRAUN SURGICAL, S.A.·Product code GAM·May 26, 2021

    EXTENSION SET, 17 INCH, 0.2 MICRON FILTER, CLAVE(TM) Y-SITE, SECURE LOCK

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·April 14, 2026

    ACCOLADE 132 SIZE 4.5

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·May 20, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 26, 2014

    AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Other ·INVACARE·Product code FNG·June 3, 2011

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·May 26, 2023

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·April 20, 2018

    50 Portal Vein Cannula REF 61.110.10.030 Size: Fr 10 Length: 12 Inches LL Connector LOT 120493 NON STERILE MEDDEV USA, INC. 100 Highland Park Village/Suite 200 DALLAS, TEXAS 75205 For use in humans. No indication of use is on the label. However, the device can be used for infusion.

    FDA Recall
    Terminated ·MEDDEV USA, INC.·Product code KDH·May 10, 2012

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 31, 2024

    CAPIOX HOLLOW FIBER OXYGENATOR/ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DTZ·January 31, 2024

    CAPIOX®RX

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·December 9, 2024

    CAPIOX RX OXYGENATOR

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·July 5, 2018