Planmeca Compact i5 User Manual page 9

32.3.1
32.3.2
32.3.3
32.3.4
32.3.5
32.3.6
32.3.7
32.3.8
32.3.9
32.3.10
32.3.11
32.3.12
32.3.13
32.3.14
32.3.15
32.3.16
32.3.17
32.4 Viewing help and error message history.................................................................................... 290
33 Consumables..........................................................................................................................................294
34 Disposal.................................................................................................................................................. 300
35 Technical information..............................................................................................................................301
35.1 Technical specifications..............................................................................................................301
35.2 Instrument classifications........................................................................................................... 304
35.3 Dimensions.................................................................................................................................305
35.3.1
35.3.2
35.3.3
35.3.4
35.3.5
35.3.6
35.4 Planmeca Compact i dental unit water consumption..................................................................311
36 Certifications........................................................................................................................................... 313
36.1 CE...............................................................................................................................................313
36.2 EU Declaration of Conformity for PlanID RFID-reader............................................................... 313
36.3 FCC Class B Notice for wireless foot control..............................................................................313
36.4 FCC Class B Notice for PlanID RFID-reader..............................................................................313
36.5 Industry Canada (IC) Compliance Statement.............................................................................314
36.6 Industrie Canada (IC) Déclaration de conformité....................................................................... 314
36.7 RF Exposure...............................................................................................................................314
User's manual
General error messages............................................................................................ 277
Power supply related error messages........................................................................279
Control panel related error messages........................................................................281
Instrument related error messages............................................................................ 281
Instrument multiplexer related error messages..........................................................282
Suction holder related error messages...................................................................... 283
Foot control related error messages.......................................................................... 284
Operating light related error messages......................................................................285
Separator system related error messages................................................................. 285
Patient chair related error messages......................................................................... 286
Main CPU related error messages.............................................................................286
Headrest related error messages...............................................................................287
ActiveAqua related error messages........................................................................... 288
Water leak related error messages............................................................................ 289
Maintenance related errors........................................................................................ 289
Software upgrade error messages.............................................................................289
Error messages generated by control panel.............................................................. 290
Positioning of patient, dentist and assistant............................................................... 305
Patient area................................................................................................................306
Over-the-patient delivery with balanced instrument arms.......................................... 308
Over-the-patient delivery with hanging-tube instruments...........................................309
Side delivery with hanging-tube instruments..............................................................310
Cart............................................................................................................................ 311
Table of contents
Planmeca Compact i