BEUDAMED
    265 results · 44ms · 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 Status: Injury ×

    NEUROTHERM¿ RF NEEDLE

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXI·August 25, 2015

    DISPOSABLE GROUNDING PAD W/OUT CABLE

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·August 25, 2015

    NEUROTHERM EPIDURAL CATHETER

    FDA Adverse Event
    Injury ·NEUROTHERM, INC.·Product code BSO·June 10, 2014

    4 LESION NT2000¿ PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·December 15, 2017

    RF DISPOSABLE GROUNDING PAD

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·November 29, 2017

    3 LESION NT1100¿ PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·December 4, 2017

    3 LESION NT1100¿ PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·December 4, 2017

    4 LESION NT2000¿ PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·December 22, 2017

    3 LESION NT1100¿ PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·December 14, 2017

    NEUROTHERM ACUTHERM DECOMPRESSION CATHETER

    FDA Adverse Event
    Injury ·NEUROTHERM, INC.·Product code GEI·December 8, 2014

    NEUROTHERM DISPOSABLE GROUNDING PAD

    FDA Adverse Event
    Injury ·NEUROTHERM, INC.·Product code GXD·November 21, 2014

    NEUROTHERM DISPOSAL RF CANNULA

    FDA Adverse Event
    Injury ·NEUROTHERM, INC.·Product code GXD·December 1, 2014

    NEUROTHERM DISPOSABLE RF CANNULA

    FDA Adverse Event
    Injury ·NEUROTHERM, INC.·Product code GXD·December 1, 2014

    RF DISPOSABLE GROUNDING PAD

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·November 20, 2017

    NEUROTHERM¿ SL PREMIUM CURVED RF NEEDLE, 20G, 15CM

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXI·November 8, 2017

    4 LESION NT2000¿ PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·November 27, 2017

    4 LESION NT2000¿ PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·December 22, 2017

    NT500 PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·December 18, 2017

    NEUROTHERM¿ RF NEEDLE

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXI·August 25, 2015

    4 LESION NT2000¿ PAIN MANAGEMENT RF GENERATOR

    FDA Adverse Event
    Injury ·NEUROTHERM, INC·Product code GXD·December 15, 2017