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

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    Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger Kit

    FDA 510(k)
    FDA Class 2 ·Neurology

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·December 20, 2018

    STIMQ PERIPHERAL NERVE STIMULATOR (PNS) SYSTEM

    FDA Adverse Event
    Injury ·STIMWAVE TECHNOLOGIES INC.·Product code GZF·April 1, 2019

    Speedlock

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657037570·DeBakey, Maryland, Curved, 5mm, Atraumatic Teet...

    Speedlock

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657044691·Metzenbaum, 5mm, Curved Handle: 1366 Standard M...

    Speedlock

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657058131·Babcock-DeBakey, 10mm, Atraumatic Serrations Ha...

    Speedlock

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657048453·Allis Atraumatic Clamp, 5mm, TC Inserted Jaws H...

    Speedlock

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657032889·Maryland, 5mm, Cross Serrations Handle: 1366 St...

    I-LIPO, MODELS A00-1238 (230V), A00-1239 (120V)

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

    BD NEXIVA DIFFUSICS CLOSED IV CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BIZACT

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·June 18, 2019

    COULTER® LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·June 14, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 30, 2011

    SILICONE ADVANCED OPTIC-VIOLET SHIELD

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·September 17, 2008

    BIZACT

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·March 8, 2018

    BIZACT

    FDA Adverse Event
    Malfunction ·COVIDIEN MFG DC BOULDER·Product code GEI·April 30, 2024

    BIZACT

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020

    BIZACT

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020

    BIZACT

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·October 19, 2020