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

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    NuVasive® Camber Laminoplasty System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·00842331121845·Titanium Rhoton Bipolar Forceps, round handles,...

    ELITE MPX LASER SYSTEM WITH CRYO C

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

    DESARA MESH MODEL: CAL-DS01

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

    MAXIMBIO CLEARDETECT COVID-19 ANTIGEN HOME TEST

    FDA Adverse Event
    Malfunction ·MAXIM BIOMEDICAL, INC.·Product code QKP·September 8, 2022

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 19, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 14, 2013

    CIDEX OPA SOLUTION

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON MEDICAL LTD.·Product code MED·September 26, 2008

    PROAQT SENSOR

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code DXG·August 18, 2025

    PROAQT SENSOR

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code DXG·August 18, 2025

    MOZEC¿ RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·September 20, 2022

    MOZEC¿ RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·September 20, 2022

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 7, 2016