Trackit Mk3 User Manual
12
1. 4 The system and its parts
The Trackit Mk3 recorder is a m ult i- channel
1
am bulatory elect roencephalograph designed for use in
a variet y of m onit oring applications, including t hose concerned with neurological and sleep disor-
ders.
Note
1
: Trackit Mk3 is available in a num ber of versions, including a 32- channel ( Trackit -32/ 0 or
Trackit - 24/ 8) , a 24- channel ( Trackit 24/ 0) and a 12- channel ( Trackit- 24/ 0) . The version is dis-
played on the Trackit Mk3 LCD at swit ch- on. This m anual applies to all versions, t he only difference
being the num ber of channels.
The Trackit Mk3 recorder com prises the following com ponent s:
Recorder
Trackit - 32/ 0 ( 32 EEG) part num ber 1186
Trackit - 24/ 0 ( 24 EEG) part num ber 1187
Trackit - 12/ 0 ( 12 EEG) part num ber 1189
Trackit - 20/ 4 ( 20 EEG, 4 POLYGRAPHI C) part num ber 1184
Trackit - 18/ 8 ( 18 EEG, 8 POLYGRAPHI C) part num ber 1185
Trackit - 24/ 8 ( 24 EEG, 8 POLYGRAPHI C) part num ber 1188
Recorder wit h internally fitt ed wireless Bluet oot h opt ion
Trackit - 32/ 0 ( 32 EEG) part num ber 1171
Trackit - 24/ 0 ( 24 EEG) part num ber 1172
Trackit - 12/ 0 ( 12 EEG) part num ber 1174
Trackit - 20/ 4 ( 20 EEG, 4 POLYGRAPHI C) part num ber 1169
Trackit - 18/ 8 ( 18 EEG, 8 POLYGRAPHI C) part num ber 1170
Trackit - 24/ 8 ( 24 EEG, 8 POLYGRAPHI C) part num ber 1173
Patient connect ion unit (PCU) Clickon
PCU- clickon Short part num ber 1181
Patient connect ion unit (PCU) Cabled
PCU- cabled 24/ 0 part num ber 1104
PCU- cabled- Extended 32/ 0 (universal) part num ber 1136
Cable, PCU 32ch 1m part num ber 1106
Cable, PCU 32ch 0.5m part num ber 1105
Cable, USB 3m part num ber 1277
Trackit Mk3 st rap, adult part num ber 1117
Trackit Mk3 st rap, child part num ber 1118
Trackit Mk3 bag wit h PCU-clickon part num ber 1259
Trackit Mk3 set up soft war e part num ber 1009
Trackit Mk3 User Manual part num ber 1114
Bat t ery Box PP3 part num ber 1111
Bat t ery Box PP3- Sm all part num ber 1140
Bat t ery Box Li part num ber 1112
1. 5 Specifications and safety
Refer to Appendix 1 for specifications.
The syst em has been certified and com plies wit h the following standards:
EN60601-1 and
European st andard for m edical elect rical equipm ent , general re-
quirem ent s and EEG syst em s.
UL60601- 1: 2003 USA standard for m edical elect rical equipm ent, general require-
CAN/ CSA 22.2 No 601.1 M90 Canadian st andard for m edical elect rical equipm ent, general re-
EN60601-1-2: 2001 European st andard for m edical elect rical equipm ent, EMC require-
Conduct ed Em issions, Group 1, Class B
Radiated Em issions, Group 1, Class B
Elect rostat ic Discharges