BEUDAMED
    23 results · 27ms · Sources: EU EUDAMED, US FDA

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    ARTHREX SPEEDCINCH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NexxZr™ T / D-100-30-NT-A350-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271112538·

    ihcDirect® Napsin A Ab, 5mL

    FDA UDI
    NOVODIAX, INC.·00850000596702·Clone R1010

    ihcDirect® Napsin A Ab, 15mL

    FDA UDI
    NOVODIAX, INC.·00850000596719·Clone R1010

    ihcDirect® Napsin A Ab Conjugate 15mL

    FDA UDI
    NOVODIAX, INC.·00850030934741·Clone R1010

    ihcDirect® Napsin A Ab Conjugate 5mL

    FDA UDI
    NOVODIAX, INC.·00850030934734·Clone R1010

    IRMA C02 MODEL 200101; IRMA AX 200601

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ULTRASTREAM CHRONIC HEMODIALYSIS CATHETER

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

    UV PHOTOTHERAPY

    FDA Adverse Event
    Injury ·UNK·Product code FTC·January 27, 2021

    UV PHOTOTHERAPY

    FDA Adverse Event
    Injury ·XUZHOU KERNEL MEDICAL INSTRUMENT EQUIPMENT CO.·Product code FTC·November 30, 2022

    UV PHOTOTHERAPY

    FDA Adverse Event
    Injury ·UNK·Product code FTC·January 25, 2021

    UV PHOTOTHERAPY LAMP

    FDA Adverse Event
    Injury ·ANGEL KISS LLC.·Product code FTC·February 3, 2021

    UV PHOTOTHERAPY

    FDA Adverse Event
    Injury ·UNK·Product code FTC·January 26, 2021

    UV PHOTOTHERAPY LAMP

    FDA Adverse Event
    Injury ·UNK·Product code FTC·January 29, 2021

    UV PHOTOTHERAPY

    FDA Adverse Event
    Injury ·ANGEL KISS LLC·Product code FTC·February 2, 2021

    UV PHOTOTHERAPY LAMP

    FDA Adverse Event
    Injury ·ANGEL KISS LLC.·Product code FTC·February 4, 2021

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011

    OT PING METER

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

    SCORPIO-FLEX PS X3 TIB INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code HSH·August 21, 2008

    INSPIRE 8 HOLLOW FIBER OXYGENATOR W/ INTEGRATED HARDSHELL VENOUS/CARDIOTOMY

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·July 4, 2019