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

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    AUTOJECT 2 FOR GLASSY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ArgenZ HT+ 98x22 A1

    FDA UDI
    ARGEN CORPORATION, THE·D818122837·Dental porcelain/ceramic restoration kit

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    HIROLLER ELEVATING WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    FOTONA TANDEM LASER SYSTEM

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

    TARGET DEVICE 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·March 2, 2012

    PROXIMATE** SKIN STAPLER 35 WIDE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDT·May 21, 2013

    S-ROM M HEAD 36MM+12 NON SKIRT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·June 3, 2011

    PRECISION XTRA /OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC., USA·Product code NBW·August 14, 2008

    DQO CATHETER, INTRAVASCULAR, DIAGNOSTIC

    FDA Adverse Event
    Injury ·COOK INC·Product code DQO·August 10, 2023

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    MUST MINI OC PRE-BENT TRANSITION ROD 75° Ø3.5/4X 200MM (STE)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKG·April 25, 2024