text.skipToContent text.skipToNavigation

BISx Digital Signal Processing Unit DMR in Agile

M1206545
2026859-001
Patient Monitoring
Other Patient Monitoring
GE HealthCare
Add to Wish List
Sign In & Add To Cart
Sign In & Add To Cart
Please select date
Second Opinion Approval Needed

Enter your approval number and submit to add item(s) to cart.

Approval Number

Please enter approval number

OR

Don't know your approval number? Call 800-437-1171
Enter opt 1 for the first three prompts, and have your System ID available.

If you add item(s) to cart and submit your order without the
approval number, GE will contact you before your order
can be confirmed for shipment.

Second Opinion Approval Needed

Select your approver's name and submit to add item(s) to your cart

Approver Name

Please Select Approver Name

OR

Don't know your approval number? Call 800-437-1171
Enter opt 1 for the first three prompts, and have your System ID available.

If you add item(s) to cart and submit your order without
selecting an approver, GE will contact you before your order
can be confirmed for shipment.


Product Overview

The BISx Digital Signal Processing Unit DMR in Agile is a customized designed brain monitoring interface cable intended for use in patient monitoring and other medical equipment as applicable. The 2-Channel Bispectral Index™ (BISx™) module, with host monitor cable and patient interface cable, uses the proprietary BIS™ algorithm to acquire and process EEG data, displayed as the BIS™ index. The BIS™ brain monitoring system generates a processed EEG parameter that provides a direct measure of the effects of sedatives on the brain. The BIS™ monitoring value is represented as a number from 0 to 100 that is calculated from the raw EEG obtained by a sensor placed on a patient’s forehead. The BIS™ value is used in a variety of settings, including anesthesia, critical care, and procedural sedation to provide objective information about an individual patient’s response to sedative drugs. The BISx™ system complies with the essential requirements of the Medical Devices Directive 93/42/EEC, as amended by Directive 2007/47/EC, as well as IEC 60601-2 26:2002 and IEC 60601-1-2003. It is a Type BF applied part. It has an internal optical coupling and an isolation transformer for patient isolation. It is protected against damage from defibrillation as long as the sensor is not located between the defibrillator pads and is resilient to artifact from electrosurgery.

Equivalent Item(s):

Below is more information on the equivalent item(s). Items without a hyperlink are listed for reference only and are not available for purchase online.

Equivalent Item(s)Item Details
2026859-001

2026859-001