General Warnings, Training and Safety Notices – Read This First
NanoScope Manual
DFU-0298-1, Revision 0
Page 4 of 38
4.
The manufacturer will make available on request circuit diagrams, component
part lists, descriptions, calibration instructions and other information required
for service to any Arthrex Authorized Service & Repair Center.
5.
Prior to each use, the NanoScope Console and all associated equipment must be
inspected for proper operation. Visually inspect the NanoScope Handpiece Kit
and components to ensure there are no scratches, chips or cracks.
6.
Ensure that the available mains voltage matches the mains voltage data on the
external power supply.
7.
Only use the Power Adapter provided with the NanoScope Console. Use of an
alternate or third party adapter may result in decreased battery performance or
damage to the Console.
8.
Do not expose the NanoScope Console to moisture, or operate it in a wet area, or
store liquids above the Console.
9.
Do not excessively bend or kink power supply cord.
10.
Do not excessively bend or kink the NanoScope Handpiece cable.
11.
If the NanoScope Handpiece is dropped, or the cable, connector or camera is
damaged in any way, do not use the Handpiece. Open a new, undamaged,
Handpiece.
12.
Never use the NanoScope Handpiece for an arthroscopy procedure without the
cannula in place. The Handpiece tube can easily be bent or broken if leveraged
against bone or other anatomy.
13.
Store the NanoScope Handpiece and all disposable accessories in the original
protective packaging to prevent sterile package damage during storage.
14.
Do not store the NanoScope Console where it will be exposed to temperatures in
excess of 122°F (50°C). Long term storage should be controlled at less than 68°F
(20°C) or battery life may diminish.
15.
Uncontrolled Relative Humidity (RH) environments may require use of
Electrostatic Discharge (ESD) precautions. The NanoScope System is ESD
certified to 30% RH. The NanoScope System may be susceptible to static
discharge damage when used in drier environments.
16.
Do not leave the Lithium Ion battery fully discharged after portable use. This will
severely reduce rechargeable battery life. Recharge the batteries by leaving
system connected to power supply. See Maintenance for battery servicing.
17.
Additional equipment connected to medical electrical equipment must comply
with the respective IEC or ISO standards (e.g. 60950 for data processing
equipment). Furthermore, all configurations shall comply with the requirements
for medical electrical systems (see the 3rd edition of IEC 60601-1). Any person
who connects external equipment to signal input and signal output ports or
other connectors has formed a system and is therefore responsible for the