BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    ReBOSSIS85

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973107545·TRIAL 90-SRK-170620 POLY UCCS 6X20MM

    n/a

    FDA UDI
    Ortho Development Corporation·00822409091799·Diamond Tooth Broaches Size 20

    BD PLASTIC NON-STERILE LUER-LOK¿ TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 15, 2017

    PREMIER C. DIFFICILE GDH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR , MODEL KN-550

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD SYRINGE PLASTIPAK 10ML S/SU

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·September 15, 2024

    SMALL BATTERY DRIVE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HWE·October 14, 2014

    URETEX SUPPORT PP KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·June 12, 2013

    OCEAN WET SUCTION WATER SEAL DRAIN

    FDA Adverse Event
    Other ·ATRIUM MED CORP·Product code KDQ·July 18, 2011

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·February 17, 2023

    KING LAD SILI CONE SINGLE USE, King Systems, 10 devices/case, ETO Sterile Size 5 / Adult Silicone King LAD¿ Patient Size: >70kg Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012