32.3.1 General error messages............................................................................................ 277
32.3.2 Power supply related error messages........................................................................279
32.3.3 Control panel related error messages........................................................................281
32.3.4 Instrument related error messages............................................................................ 281
32.3.5 Instrument multiplexer related error messages..........................................................282
32.3.6 Suction holder related error messages...................................................................... 283
32.3.7 Foot control related error messages.......................................................................... 284
32.3.8 Operating light related error messages......................................................................285
32.3.9 Separator system related error messages.................................................................285
32.3.10 Patient chair related error messages......................................................................... 286
32.3.11 Main CPU related error messages.............................................................................286
32.3.12 Headrest related error messages...............................................................................287
32.3.13 ActiveAqua related error messages...........................................................................288
32.3.14 Water leak related error messages............................................................................289
32.3.15 Maintenance related errors........................................................................................ 289
32.3.16 Software upgrade error messages.............................................................................289
32.3.17 Error messages generated by control panel.............................................................. 290
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 Positioning of patient, dentist and assistant...............................................................305
35.3.2 Patient area................................................................................................................306
35.3.3 Over-the-patient delivery with balanced instrument arms.......................................... 308
35.3.4 Over-the-patient delivery with hanging-tube instruments...........................................309
35.3.5 Side delivery with hanging-tube instruments..............................................................310
35.3.6 Cart............................................................................................................................ 311
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
Table of contents
User's manual Planmeca Compact i