BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    Patient Positioning Devices

    FDA 510(k)
    FDA Class 2 ·Radiology

    n.a.

    FDA UDI
    Karl Storz GmbH & Co. KG·04048551057292·Nasal Tip, metal, 20 mm

    LACTOSORB* 1.5MM SYSTEM TEMPLATE

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036078676·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694016803·MFx 125 Degree Angulated Locking Contoured Reco...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L142420120·14mm H x 24mm W x 20mm L XLIF Trial 12 degree L...

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973101857·Poly Insert MPCS, Size 4L, 20mm

    EMBOL-X ACCESS DEVICE/ AORTIC CANNULA, EMBOL-X SLIM ACCESSDEVICE/ AORTIC CANNULA, EMBOL-X GLIDE ACCESS DEVICE/ AORTIC CA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONCENTRA PROSTATE 4.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    G2X FILTER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·January 25, 2021

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·October 5, 2014

    CORAIL2 NON COL HO SIZE 15

    FDA Adverse Event
    Injury ·3003895575 DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code KWA·June 3, 2013

    UNKNOWN TRIATHLON KNEE

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·June 21, 2011