advertisement
12
Safety instructions
Warning and information labels on the device
The device casing carries the following warning and information labels.
Fig. 1 Warning and information labels on the device
000000-1322-734_GA_GB-US_120608
1
5
6
7
2
4
8
11
Safety instructions
IOLMaster
Carl Zeiss Meditec AG
07740 Jena, GERMANY
100…240 V
50/60 Hz
90 VA
IP20
000000-1322-734-01-DE-Vs02 MW IB
REF
1322-734
SN
XXXXXX
Type label
Manufacturer as per IEC 60601
Identification plate IOLMaster
REF
catalogue
SN
serial
Connection panel
XX/XXXX
REF
1477-889
SN
XXXXXX
Complies with 21 CFR
Subchapter J
000000-0000-007-US-Vs01
000000-1322-734-04-DE-Vs02
Warning
Disconnect the device from the power supply before servicing.
Warning label
Observe all safety notes and information in this manual
"Manufactured" label
Manufacturing date
XX/XXXX = Month/Year e.g. 06/2007
Identification plate
IOLMaster computer
REF
catalogue
SN
serial
Complies with 21 CFR
Subchapter J
13
000000-1322-734_GA_GB-US_120608
advertisement
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Related manuals
advertisement
Table of contents
- 7 Copyright
- 8 Trademarks
- 9 Contents
- 12 Notes on the user manual
- 12 Symbols
- 12 Purpose of this documentation
- 12 Accessibility of the user manual
- 13 Safety instructions
- 13 Compliance with standards and regulations
- 13 Instructions for installation and use
- 15 Safe operation
- 15 Electrical safety
- 15 Light emission from the device
- 15 Requirements for operation
- 16 Important when using the device
- 16 Disposal
- 16 Disposal of the product within the EU
- 17 Package contents
- 18 Warning and information labels on the device
- 20 Customer’s safety obligations
- 21 Description
- 21 Intended use of the device
- 21 Functional description
- 23 Overall view
- 24 Optional accessories
- 25 Power isolation transformer for external devices
- 26 Setting up the device for use
- 26 Installation
- 27 Electrical connection
- 28 Operation
- 28 General notes on control
- 29 Operation by touchpad and keyboard
- 30 Screen layout
- 31 Overview of buttons and shortcut keys
- 34 Menu overview
- 35 Options menu
- 35 Test eye
- 35 Lens database
- 37 Data store
- 40 Setup
- 49 Network Broker configuration (optional)
- 59 Preparing for measurements
- 59 Switching the device on
- 59 Patient Manager (New patient)
- 64 Adjusting the device to the patient
- 65 Axial length measurement [ALM] with Advanced Technology
- 67 Axial length measurement [ALM]
- 72 Measurement of corneal curvature [KER]
- 72 Keratometer measurement
- 75 Measurement of anterior chamber depth [ACD]
- 78 Determination of "white-to-white" [WTW] (optional)
- 80 Measuring the other eye
- 80 Printout of results
- 81 Generation of IOL options
- 81 Filling the IOL database
- 82 IOL calculation
- 89 Calculation of phakic implants (optional)
- 90 4-in-1 calculation
- 90 Optimisation of lens constants
- 90 Selecting lens data
- 91 Loading existing data records
- 92 Entering new data records
- 95 Starting optimisation
- 97 New patient
- 97 Working with the Patient manager
- 98 Retrieving a reading from previous measurements
- 99 Deleting a patient/measurement
- 100 Renaming a patient
- 101 Transmitting/exporting data (optional)
- 101 Exporting data to another system
- 102 Exporting data to a storage medium
- 103 Switching off the device