Emfit Tonic-Clonic Seizure Monitor Emfits's tonic-clonic seizure monitor's use is for detecting and notifying a caregiver is a person experiences an tonic-clonic seizure that causes faster, continued body movements while in bed,
Additionally, it can also monitor an individual's presence in the bed and will give notification if the monitored person leaves the bed or does not return to the bed within a preset time.
Sophisticated Signal Aquisition The movements lower frequency threshold is set to 3Hz. We have found this to reduce false positive notifications significantly. New embedded software features also improved noise signal filtering to minimise external disturbances causing false presence detection.
Notice fast movements as possible Tonic-Clonic Seizure When movements on the bed are faster than normal movements like turning, the monitor detects this as the clonic phase of tonic-clonic seizure. The notification triggers if the faster movements continue for longer than the preset delay. The delay can be set to 10, 13, 16, 20 seconds.
Product overview The Emfit tonic-clonic seizure monitor consists of two main components: a flexible and durable bed sonsor placed under the mattress and a bed-side monitor wirh sophisticated embedded software. Together they detect the micro-movements of a person lying on the bed - even the heart beat, and the faster movements such as muscle spasms when a person has a tonic-clonic seizure. There are no particular weight limits: sensitivity can be adjusted for a child 2-12 years, adolescent 12-21 yeras, or adult.
The monitor can be placed next to a bed, or on the wall using the included fastening bracket. It operates with x x AA 1.5v batteries.
Interface with other systems The monitor has an audible alarm with adjustable volume and a dry-contact output (NO and NC) for connection to a wireless transmitter or nurse call system.
About CE Marking Emfit Tonic-Clonic Seizure Monitor (Device model D-1090-2G and bed sensor model L-4060SL) is a class 1 medical device. It complies with the essential requirements of EMC directive 2004/108/EC, CE mark directive 93/68/EEC and Medical Device Directive 93/42/EC and carries the CE marking accordlingly.