Zeiss opmi lumera 700 User manual

Carl Zeiss
OPMI LUMERA®700
User manual
G-30-1673-en
Version 7.3
2012-05-02

OPMI LUMERA® 700
Version 7.3
Page 2 G-30-1673-en
About this manual The instruction for use is part of the delivery package.
• Carefully read it before using the device.
• Keep it at the site of use of the device.
• Store it for the entire service life of the device.
• Pass it on to every subsequent owner or user of the device.
Orientation aids – The chapter overview at the beginning of these instructions for use pro-
vides a summary of all subjects.
– The contents of each chapter are specified in detail at the beginning of
each chapter.
– A list of abbreviations, key words and technical terms in the annex facili-
tates the search for specific terms.
Scope of application The present operating manual applies to the OPMI LUMERA 700 with soft-
ware release 2.0 and the following identification:
– Reference number 6634 (floor stand)
– Reference number 6726 (ceiling mount)
Trademarks –OPMI
®, LUMERA®, Invertertube®E, CALLISTO eye®, HaMode®,
Superlux®, RESIGHT®, VISULUX®, VisionGuard®and MediLive®Trio,
ZALIGN
® and K TRACK® are registered trademarks of Carl Zeiss.
–SCI
™(Stereo Coaxial Illumination) and MEDIALINK™100 are trademarks
of Carl Zeiss.
Manufacturer
Subject to changes in design and scope of delivery and as a result of ongoing
technical development. Printed in Germany.
Copyright © Carl Zeiss Meditec AG 2012
All rights reserved. Reprints and reproductions, including excerpts, are not
permissible. However, this manual may be digitized and archived for internal
use. Access to this data by third parties is not permissible and must be pre-
vented.
Carl Zeiss Meditec AG
Goeschwitzer Strasse 51-52
07745 Jena
Germany
Fax: + 49 (0) 7364 - 20 4823
E-Mail: [email protected]
Internet: www.meditec.zeiss.com

OPMI LUMERA® 700
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Chapter Overview
Chapter: Safety Measures 5
Chapter: System Overview 47
Chapter: Preparations for use 107
Chapter: Operation 161
Chapter: What to do in the event of malfunctions 239
Chapter: Care and Maintenance 255
Chapter: System Data 271
Chapter: Annex / Options 305
Chapter: Indexes 407

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OPMI LUMERA® 700 Safety Measures
Safety Measures
Key to symbols ..................................................................................7
Hazard symbols ...........................................................................................7
Information symbols....................................................................................7
Target group .....................................................................................8
Field of application ............................................................................8
Intended use ...............................................................................................8
Normal use..................................................................................................8
Notes for the operator.....................................................................10
Requirements for operation.............................................................13
Prior to the very first use............................................................................13
Before every use........................................................................................13
During use.................................................................................................15
After every use ..........................................................................................16
Liability and warranty......................................................................17
Measures to prevent phototoxic injury ............................................18
Illumination characteristics (spectral composition)......................................18
Illumination intensity .................................................................................18
Angle of illumination .................................................................................19
Focus of the light source ...........................................................................19
Exposure time to light................................................................................20
Safety devices..................................................................................24
Symbols and labels on the device ....................................................30
Microscope labels......................................................................................30

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Labels on the suspension system............................................................... 32
Labels on the lamp housing ...................................................................... 42
Device connector signs ............................................................................. 44

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OPMI LUMERA® 700 Safety Measures
Key to symbols
We would like to inform you about safety aspects which must be observed
when handling this device. This chapter contains a summary of the most im-
portant information concerning matters relevant to instrument safety.
Hazard symbols
The following safety information has been incorporated into the instructions
for use. Please note this information and be particularly careful in these cases.
Information symbols
The following information symbols are used in these instructions for use:
–Listing
Requirements for an action
• Prompt for action
Result of an action
Additional information and hints
WARNING Warning label, which may refer to fatal injuries or severe injuries if pre-
cautions are not followed.
CAUTION Indicating a hazard, which may lead to moderately severe injuries
if risks are not avoided.
NOTE Warning label, which may refer to minor injuries and property damages
if precautions are not followed.

Safety Measures OPMI LUMERA® 700
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Target group
These instructions for use are intended for physicians, nurses and other med-
ical staff who prepare, operate or maintain the system after the appropriate
training and in accordance with the instructions given in these instructions for
use. It is the duty of the customer or institution operating the system to train
and instruct all staff using the system.
Installation and service work not described in these instructions for use must
only be performed by specialists from Carl Zeiss.
Field of application
Intended use
OPMI LUMERA 700 is a surgical microscope intended for the illumination and
magnification of the surgical area and for the support of visualization in sur-
gical procedures in the field of ophthalmology.
Normal use
In line with the intended use of the system, you can use it for surgical proce-
dures on both the anterior segment of the eye (e.g. cataract, cornea, glau-
coma) and the posterior segment of the eye (retina, vitreous).
The system-integrated SCI illumination provides an optimum red reflex and
delivers a sharply defined, high-contrast image of the patient's eye. The freely
programmable foot control panel or, alternatively, the handgrips ensure max-
imum operating comfort for the surgeon who can configure all settings re-
quired to meet his/her specific needs. In addition, the OR staff can configure
the microscope, the integrated SD 3CCD/HD 3CCD camera or change the SD/
HD video and image acquisition system using the adjustable 5.7" control
panel. The fast focus allows rapid movement over a defined travel range and

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OPMI LUMERA® 700 Safety Measures
enables the surgeon to move the focus very easily over long distances (e.g. for
folding lenses) and back to its initial position. Assistant functions such as the
keratoscope, the data injection system or the integrated slit illuminator ex-
pand the surgeon's scope of work. After completion of the surgical proce-
dure, the system can be reset to the selected, freely programmable starting
values via the standby position or reset function to ensure an optimum
starting position for the next surgery.
The system is available as a mobile and as a ceiling-mounted surgical micro-
scope. It can be supplemented by various accessories and can be prepared for
sterile use by attaching resterilizable caps, handgrips and sterile drapes. For
attachment and alignment of a 22" TFT monitor, CALLISTO eye or an oper-
ating light, the ceiling.mounted surgical microscope can be fitted with an ad-
ditional carrier arm system.
The system is intended for use in offices, hospitals or other human medicine
institutions. For disposal, please observe these instructions of use as well as
the applicable legal regulations in your country.

Safety Measures OPMI LUMERA® 700
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Notes for the operator
• Prior to using the device for the first time, please read the instructions for
use thoroughly. Also ensure to read the instructions of accessory tools.
• Only personnel who have undergone training and instruction are allowed
to use this instrument. It is the responsibility of the customer or institution
operating the equipment to train and instruct all staff using the equip-
ment.
• Only operate the device within the scope of its intended use.
• Please keep these instructions for use where there are easily accessible at
all times for the persons operating the system.
• Only personnel who have been appropriately briefed are allowed to con-
trol the surgical microscope via CALLISTO eye (option). Any change in the
focus and zoom setting via CALLISTO eye may lead to unwanted move-
ment at the surgical microscope during application (e.g. in the OP mode).
• Please observe all symbols and labels attached to the device! (see page 30)
• Observe the legal regulations for accident prevention and occupational
health and safety applicable in the country concerned.
• This system must not be modified without the manufacturer's approval. If
the system is modified, suitable inspections and testing must be complet-
ed to ensure that it can still be used safely.
The manufacturer is not liable for damage caused by unauthorized per-
sons tampering with the system. Furthermore, this will forfeit any rights
to claim under warranty.
• Modifications and repairs of this device or any equipment operated to-
gether with this device may only be performed by Carl Zeiss service staff
or other persons authorized by Carl Zeiss.
• Connect the system to a special emergency backup power supply in ac-
cordance with the regulations and directives applicable in the country of
use.
• Ensure that the installation requirements and the operation of the device
concur with the surgical conditions:
– minimum vibration
– clean environment
– do not use the device under extreme mechanical stresses
• Do not use any power-operated device that is part of the delivery scope