BEUDAMED
    55 results · 20ms · 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 ×

    Kit, Assay, Estrogen Receptor

    FDA Pre-Market Approval
    FDA Class 3 ·FLUORO-CEP{R} ESTROGEN ASSAY REAGENT

    Kit, Assay, Estrogen Receptor

    FDA Pre-Market Approval
    FDA Class 3 ·FLUORO-CEP{R} ESTROGEN ASSAY REAGENT

    Kit, Assay, Estrogen Receptor

    FDA Pre-Market Approval
    FDA Class 3 ·FLUORO-CEP{R} ESTROGEN ASSAY REAGENT

    SWANSON

    FDA UDI
    WRIGHT MEDICAL TECHNOLOGY, INC.·00840420129222·

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989051568·UPPER RIGHT SECOND MOLAR TRIMLINE BAND SIZE 15

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707031970·WEB 1ST MOLAR BANDS n.LR 15

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955932809·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955931703·Percutaneous Transluminal Angioplasty Balloon C...

    JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 14 OTW

    FDA UDI
    OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955930607·Percutaneous Transluminal Angioplasty Balloon C...

    Plateau-X Spacer System

    FDA UDI
    Life Spine, Inc.·00190837012380·

    MODIFIED CHERNE CAD DETECTOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·June 19, 2009

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·June 8, 2009

    MAVERICK2 MONORAIL PTCA CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·April 19, 2007

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·AED Plus and Fully Automatic AED Plus

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·AED 3™

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·ZOLL AED Plus and ZOLL Fully Automatic AED Plus

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·AED Plus and Fully Automatic AED Plus

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·AED Plus and Fully Automatic AED Plus

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·AED 3 defibrillator