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EEG System Video - 64 Channel

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45 views4 pages

EEG System Video - 64 Channel

Uploaded by

galibmadavi
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
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TSN: 126108 Approved Date: 2022-05-16

EEG System, Video (64 Channel)


S.N. Purchaser’s Specifications
EEG System, Video (64 Channel)
Manufacturer
Brand
Type / Model
Country of Origin
1 Description of Function
1.1 An electroencephalograph uses electrodes placed on a patient’s scalp to measure, amplify, display in
graphic form, and record the weak electrical signals generated by the brain. Electroencephalography is
useful in observing and diagnosing a variety of neurologic conditions, including epilepsy, related
convulsive disorders, and brain death. It can also be used to evaluate psychiatric disorders and
differentiate among various psychiatric and neurologic conditions. In addition, electroencephalographic
studies can assist in localizing tumours or lesions on or near the surface of the brain.
1.2 In video-EEG, you are videotaped at the same time as your EEG is recorded. The recording is carried
out for a long period of time, often several days. The doctor usually views the video and EEG images
side by side on a split screen. In this way the doctor can see precisely how your behaviour during
seizures is related to the electrical activity in your brain.
2 Operational Requirements
2.1 EEG System complete with software for acquisition, review and the compatible computer with
necessary interface and printer with a high-resolution video camera and long-time imaging storage is
required.
3 System Configuration
3.1 EEG Monitors, Video, 64 Channels complete with accessories.
4 Technical Specifications
4.1 64 Channel Video EEG Monitoring System:
 64 channel digital EEC system, user-friendly marking of events during recording/ review.
 Automatic montage selection with provision for questioned montages during acquisition and
review.
 Split screen capabilities to view live as well as review data.
 Complete digital control over sensitivity filter settings and photic stimulator sequences.
 Continuous impedance testing of electrodes during acquisition video data editing capabilities
with and without EEG data.
 EEG video data recording facility on CD/DVD in readable format on other PC’s without use of
special software.
 Patient data management and reporting software.
 Video and EEG data storage capability of at least 48 hours on the hard disk.
 Automatic and manual event detection software and notification of event occurring by alert
massage or by triggering an external device.
 Photic stimulator with adjustable stand.
 Spike detection software.
4.2 Two high definition colour digital video cameras (min 5 mega pixels) with following capabilities:
 Securely wall mountable.
 PAL format.
 Auto Eris and auto tracking facility.
 One camera with zero lux facility.
 Infra-red illuminator
 Zoom of 18 x or more
S.N. Purchaser’s Specifications
4.3 64 Channel amplifiers shall be provided.

4.4 CMRR must be > 110dB.

4.5 Noise < 2uV peak to peak.

4.6 Input Impedance > 100Mohm.

4.7 16bit ADC resolution voltage of 0.153uV.

4.8 Low filter adjustable between 0.16 to 5Hz.

4.9 High Filter Adjustable between 50 to 100Hz.

4.10 Notch Filter adjustable to software.

4.11 Acquisition Sensitivity from 1 microvolt per mm to 2000 microvolt per mm.

4.12 Networking facility.

4.13 PC:
 Core Duo / Core i5 1.8 GHz with 2GB RAM or better.
 350-400GB HDD.
 USB ports with combo drives.
 Optical Mouse.
 Multimedia Keyboard compatible with latest Windows OS.
 21” LCD TFT display.
4.14 Acquisition Software:
 Facility to combine all users defined settings into templates or protocol, for use in different
applications.
 Facility for individual channel control, customization of montages, along with re-montage
capabilities.
 Must display a graphical view of the current montage during the EEG recording.
 Facility to define new sensors must be possible as standard i.e. assign to amplifier inputs, define
traces in a mintage, define calculated channels (Average, Source / Laplacian), or define trends.
 Facility to click any point to display corresponding traces & Slide pointer to change displayed
duration of the overview.
 Facility for sortable list of all events placed in the recording, both automatically and manually.
Facility to review and add events to recorded traces.
 Facility for automatic time counters and event insertion during hyperventilation.
Facility to controlled display sensitivity for user-defined value.
 Facility to file zip.
 Facility of configurable time base.
 Spike &seizure software.
4.15 Review Software:
 Paging facility as automatic paging, Mouse controlled paging and/ or Keyboard paging.
 Playback of EEG for one or more channels.
 Facility for zoom/magnify EEG trace.
S.N. Purchaser’s Specifications
 Facility for copy &paste of EEG or trends to reports and presentations.
 Facility for viewing several recordings in tiled or cascading windows.
4.16 Patient Administration Software:
Network supported patient and test management software, archive to CD or DVD, powerful search,
patient folder, and workspaces.
4.17 DICOM ready System.

5 Accessories, spares and consumables


5.1 Accessories:
 EEG Cable (with extra one cable) with connections and 5 sets of Electrodes.
 100 boxes of conducting paste for EEG
 5 sets of medium, small and large caps.
 Customized Trolley.
 All mountings.
 Re-writable DVDs-100Nos. and paper for 1000 EEGs.
 Compatible Laser Printer with 600 DPI resolution and A4 size printing facility – 01 no.
5.2 All standard accessories, consumables and parts required to operate the equipment, including all
standard tools and cleaning and lubrication materials, to be included in the offer. Bidders must specify
the quantity of every item included in their offer (including items not specified above).
6 Operating Environment
6.1 The product offered shall be designed to be stored and to operate normally under the conditions of the
purchaser's country. The conditions include Power Supply, Climate, Temperature, Humidity, etc.
6.2 Power supply: 220 – 240VAC, 50Hz fitted with appropriate plug. The power cable must be at least 3
metre in length.
6.3 UPS of suitable ratings with voltage regulation, spike protection and maintenance free batteries for 30
minutes back-up shall be supplied with the system.
7 Standards and Safety Requirements
7.1 Must submit ISO13485:2003/AC:2007 for Medical Devices AND

7.2 CE (93/42 EEC Directives) or USFDA approved product certificate.

7.3 Shall be certified to be meeting the safety standards IEC- 60601-2-26 PART 2: Particular requirements
for safety of EEG Systems.
8 User Training
8.1 Must provide user training (including how to use and maintain the equipment).
9 Warranty
9.1 Comprehensive warranty for 2 years after acceptance.
10 Maintenance Service during Warranty Period
10.1 During warranty period supplier must ensure preventive maintenance and corrective/breakdown
maintenance whenever required.
11 Installation and Commissioning
11.1 The bidder must arrange for the equipment to be installed and commissioned by certified or qualified
personnel; any prerequisites for installation to be communicated to the purchaser in advance, in detail.
12 Documentation
12.1 User (Operating) manual in English.
12.2 Service (Technical / Maintenance) manual in English.
12.3 List of important spare parts and accessories with their part numbers and costing.
12.4 Certificate of calibration and inspection from factory.
S.N. Purchaser’s Specifications
12.5 Must submit valid manufacturer's authorization letter

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