Chapter 8 Specifications
8.1 Specifications
69
8
Power cord
• 100-120V regions
UL-listed detachable power cord set (3 conductor grounding Type SVT, AWG 18,
3m long maximum, rated at 125V AC minimum)
• 230V areas
EU/EN-approved 3-conductor power cord set (3 conductor grounding Type
H05VV-F, AWG 18, 3m long maximum, rated at 250V AC minimum)
Operating conditions
Temperature: 0 to 40
°
C
Humidity: 85% RH max. (no condensation)
Altitude: 2000 m max.
Degree of pollution: Degree 2
Installation: Category II
Electric shock protection class: Class I
Indoor use only
Transport/storage
conditions
Temperature: -20 to 60
°
C
Humidity: 90% RH max. (no condensation)
External dimensions and
weight (main unit)
External dimensions: 300 (W) x 338 (H) x 384 (D) mm
Weight: Approx. 12 kg
Safety standards
When using with the
following attachments:
• D-LH
precentered
lamphouse
• D-DH digital
imaging head M
• D-CB C-BOX
• D-NID6 sextuple
DIC nosepiece
• C-HS hand switch
• Specified adapter
for C-Box
• UL-Listed Product (UL61010A-1)
• Meets FCC 15B Class A requirements.
This equipment has been tested and found to comply with the limits for a Class A
digital device, pursuant to Part 15 of the FCC Rules.
These limits are designed to provide reasonable protection against harmful
interference when the equipment is operated in a commercial environment.
This equipment generates, uses, and can radiate radio frequency energy and, if not
installed and used in accordance with the instruction manual, may cause harmful
interference to radio communications.
Operation of this equipment in a residential area is likely to cause harmful
interference in which case the user will be required to correct the interference at his
own expense.
• This class A digital apparatus complies with Canadian ICES-003.
Cet appreil numérique de classe A est conforme à la norme NMB-003 du Canada
(NMB-003).
• This group1 class B digital apparatus complies with Australian EMC
(AS/NZS2064).
CE Marking
• Meets EU IVDD (In vitro diagnostic medical device Directive) requirements.
(GM-approved: In vitro diagnostic medical device)
• EMC
Meets EU EMC Directive (EN61326) requirements.
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