BEUDAMED
    10,000 results · 40ms · 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 ×

    FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) SYSTEM, INCLUDING FAD CATHETER KIT AND FAD INTRODUCER NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VivaChek™ Fad Blood Glucose Monitoring System, VivaChek™ Fad Smart Blood Glucose Monitoring System, VivaChek™ Fad Sync Blood Glucose Monitoring System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SOLEUS POWERED WHEELCHAIR, MODEL FAD-2

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    RESONANCE STENT SET

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FAD·March 2, 2020

    FUNCTIONAL ANESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·KYPHON, INC.·Product code BSP·March 9, 2006

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180163829·RETRACTOR BRITETRAC RIGHT ANDLED DOWN STRAIGHT ...

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00198506088452·ELMED FIBER OPTIC BRITETRAC RETRACTOR, BLUE SIL...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180163812·1" (25MM), 6" (150MM) ELMED FIBER OPTIC BRITETR...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180184411·BriteTrac Retractor, 1' x 6", with Fiberoptics,...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180169029·ELMED FIBER OPTIC BRITETRAC RETRACTOR, 1-1/4" X...

    Surgical Direct

    FDA UDI
    Surgical Direct, Inc.·B382SD12411FADS0·6" Fiber Optic Bariatric Retractor, Blue Silico...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180169012·ELMED FIBER OPTIC BRITETRAC RETRACTOR, 5/8" X 6...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180163836·RETRACTOR BRITETRAC RIGHT ANDLED DOWN STRAIGHT ...

    ELMED INCORPORATED

    FDA UDI
    ELMED INCORPORATED·00198506088445·ELMED FIBER OPTIC BRITETRAC RETRACTOR, BLUE SIL...

    NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code BSP·October 28, 2011

    DISCYPHOR CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC·Product code BSP·July 22, 2008

    ACUITY

    FDA Adverse Event
    Injury ·VARIAN MEDICAL SYSTEMS·Product code KPQ·March 19, 2014

    SIMULIX HP MARK 2

    FDA Adverse Event
    Malfunction ·NUCLETRON BV·Product code KPQ·April 2, 1998

    RESONANCE STENT SET

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FAD·September 2, 2021

    MENTOR SILTEX GEL IMPLANTS COHESIVE II

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·January 2, 2020