BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    SYSTEM 2000 REPLACEMENT BATTERY, SYSTEM 2000-EXTENDED RUN REPLACEMENT BATTERY

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517400451·CoRoent XL, 14X18x50mm 8°

    Ophthalmic Forceps

    FDA UDI
    KATENA PRODUCTS, INC.·00841668106020·GILLS-COLIBRI FORCEPS SHARP

    Endoscope Sterilization Tray

    FDA 510(k)
    FDA Class 2 ·General Hospital

    EXTENDED MEASUREMENTS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PATHROMTIN SL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017

    PATHROMTIN SL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017

    UNKNOWN FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·March 17, 2022

    PATHROMTIN SL (RILIBAK)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·January 4, 2023

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code DXY·February 9, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 22, 2014

    SELUTE PICOTIP

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVN·January 6, 2011