BEUDAMED
    56 results · 23ms · Sources: EU EUDAMED, US FDA

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    Idys ALIF ZP 3DTi

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Pantheon System

    FDA UDI
    ADLER ORTHO SPA·08050880238118·Pantheon Shaft L50mm

    STRABISMUS SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055971·STRABISMUS SCISSORS WITH GOLD SCREW CURVED BLAD...

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG

    10PW - Idaho Body Fluid

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588009209·10PW - Idaho BFKNSTD

    REAADS IGA ANTI-PHOSPHATIDYLSERINE SEMI-QUANTITATIVE TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    COZART RAPISCAN ORAL FLUID DRUG TEST - OPIATE/METHADONE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    GYNECARE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTO·August 6, 2018

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 6, 2018

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·August 6, 2018

    GYNECARE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTO·August 6, 2018

    SHILEY DISPOSABLE CANNULA LOW PRESSURE

    FDA Adverse Event
    Injury ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code JOH·April 20, 2010

    SHILEY DISPOSABLE CANNULA LOW PRESSURE

    FDA Adverse Event
    Injury ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code JOH·April 20, 2010

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·UNKNOWN MANUFACTURING FACILITY·Product code FKX·February 7, 2012

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DTK·June 30, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DTK·June 30, 2014

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·August 3, 2018

    PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·August 3, 2018

    GYNECARE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTO·August 6, 2018