BEUDAMED
    23 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    CLARITY SYSTEM II

    FDA 510(k)
    FDA Class 2 ·Neurology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150652·K-WIRE - SINGLE TROCAR THREADED 2.0mm DIA x 200mm

    MATRYX INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Metacross OTW PTA Balloon Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENTRUST VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 9, 2013

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·January 4, 2011

    POLYSXIAL SCREW-SOLID 5.5X40MM

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·July 18, 2014

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

    METACROSS OTW PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019

    OHICHO NEO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 7, 2024

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·December 26, 2019

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·July 19, 2019

    PTA BALLOON CATHETER(OHICHO3)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·December 13, 2017

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 30, 2020

    OHICHO NEO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 31, 2025

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 28, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2018