Is an EEG (Electroencephalogram) an IVD or a Medical Device?

T

TallPaul1

This seems like it should be a fairly simple question, but I can't find a clear answer! Is an EEG an IVD? I realize that in general in vitro means in a test tube, petri dish, etc, but the full definition includes "elsewhere outside of a living organism." Taking that into consideration, wouldn't pretty much all diagnostic equipment qualify as an IVD?

Thanks in advance for any insight!

Paul
 

mihzago

Trusted Information Resource
So to perform an EEG outside a living organism, would you cut the head off and send it to a lab for a test? :lol:
 
T

TallPaul1

Wow, I thought we were a little more professional than that. However, brain waves are received and measured using cutaneous electrodes. If you aren't familiar with that term it means that the electrodes are on the outside of your skin getting back to the definition of in vitro that includes "elsewhere outside of a living organism".

Paul
 

mihzago

Trusted Information Resource
relax, I was just making a joke, sorry if it didn't come across that way. If you're too serious in this job, you'll die of heart attack at age 45.

Your cutaneous electrodes are still connected to a living organism (I know, stratum corneum are dead, but still), and performing a measurement on a living organism.
 

Ronen E

Problem Solver
Moderator
In general, IVD means that a specimen is taken from the body and then diagnosed. I'm not aware of any specimen being taken away in EEG, however it's not my speciality.

More specifically, I noticed that you posted in the US medical devices regulations forum, so I'm assuming that you are interested in the FDA classification. In that system devices are considered IVD if they fall under one of the IVD devices classification regulations. I haven't checked but I'm guessing that EEG devices are not there.
 
Last edited:
T

TallPaul1

Mihzago, Ronen E and Pads 38 - thank you all very much for your insight! I 100% agree with your feedback and greatly appreciate your confirmation. Our device is classified as a Neurological Diagnostic, but I didn't know if that and IVD had to be exclusive of each other. However, given everyone's feedback on the same side of things in addition to my intuition - I would say that it's pretty clear here.

Thanks again!

Paul
 

Marc

Fully vaccinated are you?
Leader
:topic: Years ago I was a certified EEG technologist and worked in hospitals. Back in the ink on paper days. Brings back a lot of memories.
 
T

TallPaul1

I am just getting into the EEG arena, but the technology is pretty incredible.

The company that I work for has developed some software that allows for real-time results with all of the "noise" filtered out. I can't imagine how difficult it must have been in the "ink on paper days"! Times are a changing.
 

Marc

Fully vaccinated are you?
Leader
Yup - Lots of paper. Storage was a problem. The electronics back then were quite primitive compared to today. Then again, all the machines (these days called devices, I'm sure) are are amplifiers.

I did EEGs from when I graduated high school in 1969 to 1974 when I wised up (actually my younger sister sort of knocked me up side of the head a few times and finally convinced me to) and went to college. Biology major with chemistry and anthropology minors. And I ended up in quality assurance... :naughty:
 
Thread starter Similar threads Forum Replies Date
R Qualify EEG surface electrodes as AP acc 60601-1 IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
N ECoG/EEG electrodes - Required IEC 60601-1 tests IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
N USB Powered EEG - USB provides 1 MOPP want 2 MOPP IEC 60601 - Medical Electrical Equipment Safety Standards Series 0
E Are EEG electrodes considered as one applied part? IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
R Data Analysis Software classified as MDSW IVD? EU Medical Device Regulations 3
Ed Panek Looking for help... FDA Pre Sub, IVD, Investigational level experience US Medical Device Regulations 0
T IVD Self-Test Notified Body Conformity Assessment Process EU Medical Device Regulations 0
T Clinical Study Design for IVD Self-Test (lay user) Products UK Medical Device Regulations 0
M Multiple DMRs for IVD Medical Device and FDA Regulations and Standards News 0
A CE IVD Mark - Emission certifications for unexpensive product CE Marking (Conformité Européene) / CB Scheme 1
M Class III IVD PMA Amendment to FDA Medical Device and FDA Regulations and Standards News 1
M IVD Device Design Change Medical Device and FDA Regulations and Standards News 2
BusyBee IVD relabeling UK Medical Device Regulations 2
R Selling same device as IVD and RUO US Medical Device Regulations 8
R Selling same device as IVD and RUO EU Medical Device Regulations 1
C South Korea - MFDS registration for a Chinese IVD factory Other Medical Device Regulations World-Wide 4
K IVD Usability IEC 62366 - Medical Device Usability Engineering 4
MaHoDie Regulatory compliance for IVD in india Other Medical Device Regulations World-Wide 2
S Registration of IVD in South Africa Other Medical Device Regulations World-Wide 2
T IVD Risk - destruction of patient samples - Harm to property? ISO 14971 - Medical Device Risk Management 5
T IVD Device Software - Risk Classification IEC 62304 - Medical Device Software Life Cycle Processes 16
R RUO and IVD Medical Device and FDA Regulations and Standards News 1
M UDI IVD - before submission? US Food and Drug Administration (FDA) 2
M UDI IVD Medical Device Class III US Food and Drug Administration (FDA) 1
BusyBee IVD components supplied in bulk CE Marking (Conformité Européene) / CB Scheme 1
R IVD Software FDA/CLIA doubts Medical Device and FDA Regulations and Standards News 1
R IVD software FDA and CLIA US Food and Drug Administration (FDA) 2
K Clinical Studies of MD and IVD in the US US Food and Drug Administration (FDA) 6
M Labeling IVD Class III Medical Device and FDA Regulations and Standards News 0
R IVD Label Change China Medical Device Regulations 1
R IVD Label Change Requirements Other Medical Device Regulations World-Wide 0
D IVD Accuracy and Precision Acceptance Criteria ISO 13485:2016 - Medical Device Quality Management Systems 1
K Brazil (INMETRO) for Medical Electrical and IVD Equipment? Other Medical Device Regulations World-Wide 4
E IVD devices helping labs meet CLIA/CAP QC requirements? Hospitals, Clinics & other Health Care Providers 0
R How to find the proper the fieids of IVD distributers and develop the medical device markets in Thailand? Manufacturing and Related Processes 0
S CE Marking components within IVD CE Marking (Conformité Européene) / CB Scheme 0
B IVD - GSPR checklist Other Medical Device Related Standards 0
E Does IVD need to integrate with hospital IT infrastructure? Medical Information Technology, Medical Software and Health Informatics 2
T CE-IVD mark on packaging EU Medical Device Regulations 1
A Is computing Hardware part of the IVD CE Marking (Conformité Européene) / CB Scheme 3
C IVD Metrological traceability without a reference measurement procedure General Measurement Device and Calibration Topics 11
B Looking for SSCP file of IVD devices EU Medical Device Regulations 7
B Research Use Only (RUO) IVD Medical Devices in China China Medical Device Regulations 2
B What is the difference btw RUO vs IUO for IVD in FDA guidance ? US Food and Drug Administration (FDA) 12
Y Handbook recommended lightcycler for IVD Risk Management Principles and Generic Guidelines 1
S IVD Device History Record ISO 13485:2016 - Medical Device Quality Management Systems 5
J IVD sampling sizes for buyer Reliability Analysis - Predictions, Testing and Standards 0
D Low risk IVD study in the UK, do I need MHRA approval? UK Medical Device Regulations 1
A CE-IVD Technical File with Multiple IFUs EU Medical Device Regulations 5
A Ethics Committee Review Process for IVD Products EU Medical Device Regulations 2

Similar threads

Top Bottom