263 results
·
30ms
·
Sources: EU EUDAMED, US FDA
NEUROMED -ADVANCED NEUROMODULATION SYSTEMS, INC.-
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code GZB·March 26, 2003
SPINAL NERVE STIMULATOR
FDA Adverse Event
Malfunction
·NEUROMED, INC.·Product code GZB·January 10, 1994
SPINAL STIMULATOR
FDA Adverse Event
NEUROMED, INC.·Product code GZB·February 15, 1994
NEUROSTIMULATION SYSTEM
FDA Adverse Event
Injury
·NEUROMED INC.·Product code GZB·August 12, 2023
MULTIPROGRAMMABLE NEUROSTIMULATOR RECEIVER
FDA Adverse Event
Injury
·NEUROMED, INC.·Product code GZB·December 29, 1994
EUROMED, INC.
FDA registration
EUROMED, INC.·5 products·🇺🇸 United States
NeuroX USA Inc
FDA registration
NeuroX USA Inc·1 product·🇺🇸 United States
NEUROMED DUAL OCTRODE RECEIVER
FDA Adverse Event
Malfunction
·ANS, ADVANCED NEUROMODULATION SYSTEMS·Product code GZB·November 8, 2000
SmartTwist MR Hand Drill
Device
EU MDR
·
Eu Md Class 1
·ClearPoint Neuro, Inc.·On the market·32 countries
SmartFrame XG Targeting Cannula
Device
EU MDD
·
Eu Md Class 2a
·ClearPoint Neuro, Inc.·On the market·1 country
Inflexion
Device
EU MDR
·
Eu Md Class 1
·ClearPoint Neuro, Inc.·On the market·0 countries
ClearPoint
FDA UDI
Clearpoint Neuro, Inc.·00850376007369·ClearPoint GE Compatible Fixation Frame Screws
ClearPoint
FDA UDI
Clearpoint Neuro, Inc.·00850376007550·ClearPoint Inflexion Philips Achieva HFF
ClearPoint
FDA UDI
Clearpoint Neuro, Inc.·00850359007638·SMARTFrame Scalp Mount Kit w/ TE
ClearPoint PURSUIT
FDA UDI
Clearpoint Neuro, Inc.·00850359007706·ClearPoint Pursuit, 5.9 mm OD x 250 mm Length
SmartFrame
FDA UDI
Clearpoint Neuro, Inc.·00850359007041·SMARTFrame Scalp Mount Kit w/ TE
ClearPoint
FDA UDI
Clearpoint Neuro, Inc.·00850359007805·Bladed Lancet
ClearPoint
FDA UDI
Clearpoint Neuro, Inc.·00850376007543·ClearPoint Inflexion GE 750w HFF
SmartFrame Array
FDA UDI
Clearpoint Neuro, Inc.·00850359007935·SmartFrame Array Thumbwheel Extension
Altius Patient Controller
FDA UDI
Neuros Medical, Inc.·00810118490026·