BEUDAMED
    98 results · 33ms · Sources: EU EUDAMED, US FDA

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    BriefCase

    FDA 510(k)
    FDA Class 2 ·Radiology

    Phasix

    FDA UDI
    Davol Inc.·00801741095313·Phasix ST Mesh, 10 cm x 20 cm (4" x 8"), Rectangle

    Pantheon System

    FDA UDI
    ADLER ORTHO SPA·08050880238217·Pantheon Bridging Collar Ø 26 mm for Stem Ø 12 mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694019293·6mm Hohmann Retractor

    MULTI-GUIDE

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540257697·PIN CLAMP, RIGHT

    TERUMO GAS FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    8100 VITAL SIGNS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 14, 2012

    LIFE GUARD

    FDA Adverse Event
    Malfunction ·CHURCHILL·Product code FMI·June 30, 2011

    LIFE GUARD

    FDA Adverse Event
    Malfunction ·CHURCHILL MEDICAL SYSTEMS·Product code FMI·July 15, 2011

    PARADYM

    FDA Adverse Event
    Malfunction ·SORIN BIOMEDICA C.R.M., S.R.L.·Product code MRM·January 7, 2011

    ENTRUST VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·June 15, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 15, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 2, 2010

    TOTAL ASR FEM IMP SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·October 27, 2014

    CAST CUTTER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HAB·July 1, 2011

    TI COLLAR WITH GROOVES

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MNH·July 2, 2013

    EXPRESSEW III W/O HOOK

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code LXH·April 6, 2021

    ENTRUST VR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·April 22, 2010