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

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    RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    NexxZr™ T / D-100-20-NT-C400-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271113481·

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981200862·Interbody, 11mm x 32mm x 13mm, 8 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981192877·Interbody, 11mm x 32mm x 13mm, 8 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981207984·Trial, 11mm x 32mm x 13mm, 8 deg

    MEDTRONIC SINGLE USE ESOPHAGEAL MANOMETRIC CATHETER, MEDTRONIC SINGLE USE ANORECTAL MANOMETRIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ULTRASONIC TABLETOP DOPPLER; ULTRASONIC TABLETOP DOPPLER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·March 21, 2008

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JGS·May 7, 2009

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 14, 2023

    COBAS INTEGRA (800)

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 28, 2007

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTERNATIONAL·Product code MNI·July 12, 2013

    FLEXTEND

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 5, 2012

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 4, 2023

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTERNATIONAL·Product code MNI·July 12, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·August 22, 2008

    VITROS 5,1 FS CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·June 17, 2011