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Difference between revisions of "Philips"

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[[Category:Organizations]]
 
[[Category:Organizations]]
 
[[Category:Companies]]
 
[[Category:Companies]]
Philips is a health care company that focuses only on patients' proper recovery and diagnosis treatment.
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"Philips is a health care company that focuses only on patients' proper recovery and diagnosis treatment."
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[[File:Philips.png|thumb|Philips Company Profile]]
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Founded in The Netherlands around 1891, Philips produces noninvasive hardware and end-user software.
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Philips makes tools for medical diagnosis and treatment through body/mind state interpretation and/or neurostimulation therapies.
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[[Brain Computer Interface Classification|BCI Categories]]: Open-Loop Efferent
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[[:Category:Neurosensing_Techniques|Neurosensing Technique(s)]]: EEG, EMG, fNIRS, MRI
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==Hardware==
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*[[CT_5100_Incisive|CT 5100 Incisive]]
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*[[CT_6000_iCT|CT 6000 iCT]]
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*[[Hitachi_ETG_4100|Hitachi ETG 4100]]
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*[[Incisive_CT|Incisive CT]]
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*[[Ingenia_1.5T_Evolution|Ingenia 1.5T Evolution]]
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*[[Ingenia_MR-RT_XD|Ingenia MR-RT XD]]
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*[[IQon_Elite_Spectral_CT|IQon Elite Spectral CT]]
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*[[IQon_Spectral_CT|IQon Spectral CT]]
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*[[MR_5300|MR 5300]]
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*[[MR_7700|MR 7700]]
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*[[Spectral_CT_7500|Spectral CT 7500]]
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==FDA==
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Philips has 239 medical devices registered with the FDA. Here are some of them:
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{| class="wikitable" style="margin:auto"
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|+ Examples of FDA Approved Devices ([[Philips_FDA_Devices | View List]])
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|-
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! Device ID !! Device Name !! Class !! Category !! PMA !! PMN
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|-
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| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P960042 P960042] || Device, Removal, Pacemaker Electrode, Percutaneous || 3 || Cardiovascular || True || False
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|-
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| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P960042 P960042] || Device, Removal, Pacemaker Electrode, Percutaneous || 3 || Cardiovascular || True || False
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|-
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| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P180034 P180034] || Scaffold, Dissection Repair || 3 || Cardiovascular || True || False
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|-
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| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P960042 P960042] || Device, Removal, Pacemaker Electrode, Percutaneous || 3 || Cardiovascular || True || False
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|-
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| [https://www.accessdata.fda.gov/scrIpts/cdrh/devicesatfda/index.cfm?db=pma&id=P180034 P180034] || Scaffold, Dissection Repair || 3 || Cardiovascular || True || False
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|-
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| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K201012 K201012] || System, Imaging, Pulsed Doppler, Ultrasonic || 2 || Radiology || False || True
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|-
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| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K170144 K170144] || Interventional Fluoroscopic X-Ray System || 2 || Radiology || False || True
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|-
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| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K171314 K171314] || System, Image Processing, Radiological || 2 || Radiology || False || True
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|-
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| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K172406 K172406] || System, Tomography, Computed, Emission || 2 || Radiology || False || True
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|-
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| [https://www.accessdata.fda.gov/scripts/cdrh/devicesatfda/index.cfm?db=pmn&id=K190913 K190913] || System, Image Processing, Radiological || 2 || Radiology || False || True
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|}
 
==Links==
 
==Links==
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[https://www.usa.philips.com Website]
 
[https://www.usa.philips.com Website]
 
[https://www.crunchbase.com/organization/philips-c6d9 Crunchbase]
 
[https://www.crunchbase.com/organization/philips-c6d9 Crunchbase]
 
[https://www.linkedin.com/company/philips/ LinkedIn]
 
[https://www.linkedin.com/company/philips/ LinkedIn]
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[https://twitter.com/PhilipsNA Twitter][https://facebook.com/Philips Facebook]
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[https://youtube.com/Philips YouTube]
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[https://github.com/Modernizr/Modernizr/issues/648 GitHub]
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[https://instagram.com/philips/ Instagram]

Latest revision as of 02:28, 18 April 2023

"Philips is a health care company that focuses only on patients' proper recovery and diagnosis treatment."


Philips Company Profile

Founded in The Netherlands around 1891, Philips produces noninvasive hardware and end-user software.

Philips makes tools for medical diagnosis and treatment through body/mind state interpretation and/or neurostimulation therapies.

BCI Categories: Open-Loop Efferent

Neurosensing Technique(s): EEG, EMG, fNIRS, MRI

Hardware

FDA

Philips has 239 medical devices registered with the FDA. Here are some of them:

Examples of FDA Approved Devices ( View List)
Device ID Device Name Class Category PMA PMN
P960042 Device, Removal, Pacemaker Electrode, Percutaneous 3 Cardiovascular True False
P960042 Device, Removal, Pacemaker Electrode, Percutaneous 3 Cardiovascular True False
P180034 Scaffold, Dissection Repair 3 Cardiovascular True False
P960042 Device, Removal, Pacemaker Electrode, Percutaneous 3 Cardiovascular True False
P180034 Scaffold, Dissection Repair 3 Cardiovascular True False
K201012 System, Imaging, Pulsed Doppler, Ultrasonic 2 Radiology False True
K170144 Interventional Fluoroscopic X-Ray System 2 Radiology False True
K171314 System, Image Processing, Radiological 2 Radiology False True
K172406 System, Tomography, Computed, Emission 2 Radiology False True
K190913 System, Image Processing, Radiological 2 Radiology False True

Links

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