ASI – The leader in Advanced Systems Integration | www.asimedical.net
TRiTOn
™
ADVAnceD DenTAl SySTeMS
®
2025M | 2025M/DV | 2025M/AR
17
65-2025M Rev. B
1.8 Operating environment & classification of equipment
classification of equipment (en-60601-1)
Type/Mode
classification
Types of shock protection
Class I Equipment: Chair, wall, and cart delivery systems
Degree of shock protection
TYPE B and/or TYPE BF APPLIED PART depending on order configuration
Degree of protection against water ingress
ORDINARY EQUIPMENT
Mode of operation
Intermittent
Flammable Gasses:
Not suitable for use in the presence of a flammable anesthetic mixture with air, oxygen, or nitrous oxide,
where such gasses may accumulate in concentration (closed spaces).
environmental Specifications
Temperature/Humidity
Specification
Storage/Transportation Temperature:
-40˚C to 70˚C (-40˚F to 158˚F) - Relative humidity 80%
Operating Temperature:
10˚C to 40˚C (40˚F to 104˚F) - Relative humidity 80%
Indoor Use:
Altitude up to 2,000M (6,563 ft.), installation category II, pollution degree 2. (UL 61010A-1 and CAN/
CSA C22.2, No. 1010.1-92 only)
electromagnetic compatibility (eMc)
Although this equipment conforms to the intent of the 2004/108/EC EMC Directive, all medical equipment may produce
electromagnetic interference or be susceptible to electromagnetic interference. The following are guidance and manufacturer’s
declarations regarding EMC for the Triton™ Advanced Dental System
®
.
• The Triton™ Advanced Dental System® needs special precautions regarding EMC and needs to be installed and put
into service according to the EMC information provided in the following pages.
WARninG: This equipment is intended for use by healthcare professionals only.
As with all electrical medical equipment, this equipment may cause radio interference or may disrupt the operation
of nearby equipment. It may be necessary to take mitigation measures such as re-orienting or relocating the Triton™
Advanced Dental System® unit or shielding the location.
• Portable and Mobile RF communications equipment can affect the performance of the Triton™ Advanced Dental
System®. Please use the guidelines and recommendations specified in Tables 4 and 6 (IEC 60601-1-2, Edition 3.0).
• Other Medical Equipment or Systems can produce electromagnetic emissions and therefore can interfere with
the functionality of the Triton™ Advanced Dental System®. Care should not be used when operating the Triton™
Advanced Dental System® adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the
Triton™ Advanced Dental System® should initially be observed to verify normal operation in the configuration in which
it will be used.
• The electrical cables, external power supplies and accessories listed or referenced in this manual have been shown to
comply with the test requirements listed in the following tables.
