Haag-Streit IM 900 Instruction Manual - page 4
4
DEUTSCH
ENGLISH
FRANÇAIS
ITALIANO
ESPAÑOL
NEDERLANDS
PORTUGUÊS
SVENSKA
DEUTSCH
ENGLISH
FRANÇAIS
ITALIANO
ESPAÑOL
NEDERLANDS
PORTUGUÊS
SVENSKA
© HAAG-STREIT AG, 3098 Koeniz, Switzerland – HS Doc. No. 1500.7220551.04020 – 2016 – 08
1. Safety
DANGER!
Failure to comply with these instructions may result in material damage
or pose a danger to patients or users.
WARNING!
These warnings must absolutely be complied with to guarantee
safe operation of the device and to avoid any danger to users and
to patients.
NOTE!
Important information: please read carefully.
1.1 Areas of application of the device
The device is intended for use in doctor's practices, hospitals and optometrists' and
opticians' premises.
1.2 Ambient conditions
Transport:
Temperature
Air pressure
Relative humidity
from
from
from
−40°C
500 hPa
10%
to
to
to
+70°C
1060 hPa
95%
Storage:
Temperature
Air pressure
Relative humidity
from
from
from
−10°C
700 hPa
10%
to
to
to
+55°C
1060 hPa
95%
Use:
Temperature
Air pressure
Relative humidity
from
from
from
+10°C
800 hPa
30%
to
to
to
+35°C
1060 hPa
90%
1.3 Shipment and unpacking
•
Before you unpack the device, check whether the packaging shows traces of in‑
correct handling or damage. If this is the case, notify the transport company that
has delivered the goods to you. Unpack the device together with a representative
of the transport company. Prepare a report for any possible damaged parts. This
report must be signed by you and by the representative of the transport company.
•
Leave the device in the packaging for a few hours before unpacking it (conden‑
sation).
•
Check the device for damage after it is unpacked. Return defective devices in the
appropriate packaging.
•
Store packaging material carefully, so that it can be used for possible returns or
when moving.
1.4 Installation warnings
WARNING!
•
Do not modify this equipment without authorization of the manufacturer.
Installation and repairs may only be performed by trained specialists.
Any third-party device must be connected in compliance with the
EN 60601-1 standard.
Only original HS replacement parts may be used.
The device must not be stacked or placed in close proximity to other
electronic devices.
•
•
•
NOTE!
The power supply unit's mains connector must be accessible in order
to allow for disconnection from the mains at any time!
1.5 Operation, environment
DANGER!
Never use the device in potentially explosive environments where vola-
tile solvents (alcohol, petrol, etc.) and flammable anaesthetics are in
use.
WARNING!
The device must be switched off after every use. Otherwise there is a
risk of overheating when a protective dust cover is used.
WARNING!
•
The imaging module is intended for documentation purposes. The
ocular image is critical for diagnosing a patient!
•
Before every examination, check that the automatic left to right de‑
tection works correctly from the release module!
•
The release module RM02 is affixed with strong magnets. Keep mag‑
net‑sensitive storage media (e.g. credit cards) away from the mag‑
nets!
NOTE!
This equipment must only be operated by qualified and trained person-
nel. The owner is responsible for their training. This device may only be
used in accordance with the instructions in "Purpose of use".
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