6
DEUTSCH
ENGLISH
FRANÇAIS
ITALIANO
ESPAÑOL
NEDERLANDS
PORTUGUÊS
SVENSKA
© HAAG‑STREIT AG, 3098 Koeniz, Switzerland – HS‑Doc. no. 1500.7220686.04020 – 2. Edition / 2021 – 05
• If EyeSuite is used on an external PC for the review and further
analysis of the data acquired with the device, then the PC on which
the EyeSuite software is installed may not contain any other
software which could restrict the correct operation of EyeSuite.
• Please switch the device and or external computer off if it is not to
be used for a long time.
• The device may not be transported, stored, handled or operated
outside the specified ambient conditions (see chapter 'Ambient
conditions').
• The device is to be used in a room in the medical area with
attenuated light.
• If the device is moved/transported, a functional check must be
performed in accordance with the software instructions for use.
• If the device or accessories to it are exposed to the effects of an
external force (e.g., by being accidentally knocked or dropped), this
sensitive measuring device must be promptly checked according to
the software instructions for use and, if necessary, returned to the
factory for repair.
• The selected measuring mode must be checked before every
measurement.
• Keep these instructions for use in a place where they are accessible
at all times to those working with the device.
• Warranty claims can only be made if the instructions for use have
been complied with.
• The manufacturer of the device is not liable for loss or damage due
to unauthorised handling of the same. All warranty claims arising in
this case are null and void.
• Always remove the dust cover before switching the device on. If the
cover is not removed before switching the device on it may suffer
damage due to overheating. Likewise, make sure that the device is
switched off before attaching the dust cover.
• Repairs may only be conducted by suitably trained and authorised
specialist personnel. Incorrect repairs can pose considerable risks
for operating staff and patients.
• Housing parts of the device may only be removed by suitably trained
and authorised specialist personnel.
• Only original spare parts and original accessories may be used for
repairs.
• The software must be installed by trained personnel.
• Measurements should only be taken with the forehead rest band
and chin rest shell mounted correctly.
• Extensive amounts of ametropia of the patient may be corrected
using glasses or trial lenses during the measurement. Contact
lenses may not be used for this purpose as they would lead to
inaccurate measurement results.
• The patient should be advised to open his eyelids wide during the
measurement to allow best data acquisition.
• Unstable tear film, tear film breakup or dry eye syndrome may lead
to inaccurate and or instable measurements. It is recommended to
use artificial tears in such cases.
• It is recommended to set a user name and password for every user
of the device to best protect sensitive patient data.
• It is recommended and is in the responsibility of the user to protect
sensitive patient information using the access control (password
protection) on the device.
1.7 Plausibility of the measurements
WARNING!
• Users must check measurement readings for plausibility. This
includes the checking of the A and B-scan and the cursors, which
automatically adjust to the signal, the keratometry values, the white-
to-white distance and the pupillometry, whenever one of the
measurements displays an unusually high standard deviation. The
operator must also take into account the type (e.g., posterior
subcapsular cataract) and density of the cataract when evaluating
plausibility.
