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

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    MODIFICATION TO D-TRONPLUS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TIGER Spine System

    FDA UDI
    CORELINK LLC·M7256043000·POSTED SCREW SET SCREW - CONNECTOR

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702538182·Elvarex 1/Knee High/Slant-Open Toe/Dotted 5 cm ...

    JOBST Confidence

    FDA UDI
    BSN-Jobst GmbH·04059993459995·CONFIDENCE 3/THIGH HIGH/SLANT-CLOSED TOE-FOOT F...

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702265637·Elvarex 2/Knee High/Closed Toe/Dotted 5 cm Sili...

    JOBST Confidence

    FDA UDI
    BSN-Jobst GmbH·04059993550777·CONFIDENCE 1/PANTY-BODY BANDAGE/SLANT-OPEN TOE-...

    JOBST Confidence

    FDA UDI
    BSN-Jobst GmbH·04059993541058·CONFIDENCE 2/PANTY-BODY BANDAGE/SLANT-OPEN TOE-...

    MATIRA ANTERIOR CERVICAL SYSTEM

    FDA UDI
    Kalitec Direct LLC·B07307K0130001·PLATE BENDER, UNIVERSAL

    JOBST Elvarex

    FDA UDI
    BSN-Jobst GmbH·04019702330250·ELVAREX FORTE 3/THIGH HIGH/SLANT, OPEN TOE, E-V...

    Ocata Anterior Cervical System

    FDA UDI
    Kalitec Direct LLC·B07308K0130000·Plate Bender Assembly

    Spex

    FDA UDI
    SPEX LIMITED·09420051706255·Spex Standard Lateral Head Support Head Support...

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 27, 2021

    GRAMS NYLON NONABSORBABLE SUTURE

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

    MEDTRONIC INVISX BURR HOLE LOCK, MODEL 60520

    FDA 510(k)
    FDA Class 2 ·Neurology

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 6, 2016

    ARCHITECT I1000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·June 9, 2019

    ACCURUS 600DS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·March 7, 2013

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·March 25, 2011

    FINELINE II

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code DTB·May 8, 2008

    TC pCO2 Electrodes, Model/Part #945-655-E5260, 510(k) #K043003. Product Usage: The device is intended for used with the firm's TCM series monitor. The E260mpCO2 electrode is a non-invasive device, used with the TCM series monitor to measure transcutaneous pCO2 (through the skin).

    FDA Recall
    Terminated ·Radiometer America Inc·Product code LKD·September 27, 2011