om 5184516-100 Rev. 5 2-4
Call Traffic and Transportation, Milwaukee, WI (414) 827–3449 / 8*285–3449
immediately after damage is found. At this time be ready to supply name of car-
rier, delivery date, consignee name, freight or express bill number, item damaged
and extent of damage.
Complete instructions regarding claim procedure are found in Section “S” of the
Policy & Procedure Bulletins.
3-3Regulatory Requirements
This equipment generates, uses, and can radiate radio frequency energy. The
equipment may cause radio frequency interference to other medical and non-
medical devices and radio communications. To provide reasonable protection
against such interference, this product complies with emissions limits for a Group
1 Class A Medical Devices as stated in EN 60601–1–2.
However, there is no guarantee that interference will not occur in a particular instal-
lation. If this equipment is found to cause interference (which may be determined by
switching the equipment on and off), the user (or qualified service personnel) should
attempt to correct the problem by one or more of the following measure(s):
• Reorient or relocate the affected device(s).
• Increase the separating space between the equipment and the affected device.
• Power the equipment from a source different from that of the affected device.
• Consult the point of purchase or service representative for further suggestions.
The manufacturer is not responsible for any interference caused either by the use
of interconnect cables other than those recommended, or by unauthorized
changes or modifications to this equipment. Unauthorized changes or modifica-
tions could void the user’s authority to operate the equipment.
To comply with the regulations applicable to an electromagnetic interface for a
Group 1 Class A Medical Device, all interconnect cables to peripheral devices
must be shielded and properly grounded. Use of cables not properly shielded and
grounded may result in the equipment causing radio frequency interference in vio-
lation of the European Union Medical Device directive and FCC regulations.
NOTE: Do not use devices which intentionally transmit RF Signals (Cellular Phones,
Transceivers, or Radio Controlled Products) in the vicinity of this equipment as it
may cause performance outside the published specifications. Keep the power to
these type devices turned off when near this equipment.
FOR TRAINING PURPOSES ONLY!
NOTE: Once downloaded, this document is UNCONTROLLED, and therefore may not be the latest revision. Always confirm revision status against a validated source (ie CDL).
To Next Page
Loading...
Need help?
General
