BEUDAMED
    24 results · 36ms · 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 ×

    ACUMATCH P-SERIES POROUS PRESS-FIT FEMORAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Humelock Reversed Shoulder

    FDA UDI
    FX SOLUTIONS·03701037306321·HUMELOCK REVERSED METAPHYSEAL RASP Ø36mm

    Asnis

    FDA UDI
    Stryker GmbH·07613154631414·CANNULATED SCREW

    SCFE Screw

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132114599·4.0mm X 36mm SHORT THREAD CANNULATED SCREW

    SYNERGY VLS CAP NUT MODELS 2206, 6102

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RETINADX

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    LASERPOR 030-236

    FDA Adverse Event
    Injury ·TELECTRONICS PACING SYSTEMS·Product code DTB·March 15, 1997

    LASERPOR 030-236

    FDA Adverse Event
    Malfunction ·TELECTRONICS PACING SYSTEMS·Product code DTB·March 15, 1997

    VERTE-STACK K030736, K041197

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·January 4, 2019

    TRIAGE CARDIAC TRIPLE MARKER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 12, 2018

    TRIAGE CARDIAC HS PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 22, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·February 4, 2025

    TRIAGE CARDIAC TRIPLE MARKER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code MMI·May 18, 2018

    TRIAGE CARDIAC PANEL KIT

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code JHX·April 18, 2018

    TRIAGE CARDIAC HS PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 21, 2019

    TRIAGE CARDIAC TRIPLE MARKER PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·October 5, 2017

    MONARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTN·March 28, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·March 21, 2011

    BIPHASIC LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·April 15, 2008

    TRIAGE CARDIAC TRIPLE MARKER PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·November 1, 2018