Technical Specifications | CARESTREAM Vita Flex CR System

CARESTREAM Vita Flex CR System—Specifications

and Regulatory/Safety Information

The new Vita Flex CR System effortlessly transforms your Grayscale Resolution
traditional radiography into a powerful digital imaging solution
with minimal cost or downtime. It delivers impressive image • 12-bit processed
quality at 30 or 45 plates per hour throughput (for 14 x 17 in. • 16-bit unprocessed
cassette), incredible flexibility, field-tested durability, simple
servicing and more room for care.
Storage and Operating Environments
Physical Specifications
• Weight: 25 kg (55 lb) Operation Transport/
• Dimensions (W x D x H): 68.0 x 34.0 x 45.0 cm (26.7 x Storage
13.4 x 17.7 in.)
Ambient +5 to +45 °C -23 to +66 °C
Dynamic Range temperature (+41 to (-10 to +150 °F)
+113 °F)
0 < 40 mR

Power Relative 25– 81 % 10– 86 %

humidity
• Electrical Rating: 100-240 V AC 50/60 Hz
• Maximum Power Consumption: 120 W
• Power Consumption in Standby Mode: 42 W Atmospheric 700—1060 hPa
• Power Supply Conditions: AC Power 100~240 V AC, pressure
50/60 Hz, 1.5 A

Heat Dissipation
While in Operation: 330 BTU/H (97 W)

Noise Level
• Noise Level while Operating, while Running in the
Operating State: Below 58 dBA
• Noise Level during Loading Period: Below 70 dBa

Erase Specifications
• Erase Range: 0 < 40 mR
• Erase Time 7 < 80 s (depending on screen exposure)
Technical Specifications | CARESTREAM Vita Flex CR System
Supported Cassette Sizes and Specifications

Cassette Size Plate Size Pixels Per Time to First Plates Per Hour
Millimeter [µm] Image
X Y Vita Flex 30PPH Vita Flex 45PPH

Standard Resolution

14 x 17 in. 354 430 160 52 30 45

14 x 14 in. 354 354 160 51 31 47
10 x 12 in. 252 304 160 47 34 53
8 x 10 in. 220 252 160 46 36 59
24 x 30 cm 239 299 160 47 34 54

High Resolution

14 x 17 in. 354 430 86 85 24 33

14 x 14 in. 354 354 86 83 25 35
10 x 12 in. 252 304 86 71 28 40
8 x 10 in. 220 252 86 70 29 43
24 x 30 cm 239 299 86 71 28 40

Note: The tolerance of throughput and time-to-first-image values could be ±5 %.

Regulatory European Union

• FDA • EN 60601-1: 2006 - Medical Electrical Equipment -
• CE mark Part1:General Requirements for safety and essential
• cTUVus mark performance
• EN 60825-1: 2007 - Safety of Laser Products
Health and Safety Compliance
International
The Vita Flex CR System was examined for compliance and has
classifications and licenses as follows: • IEC 60601-1: 2005 - Medical Electrical Equipment -
Part1:General Requirements for safety and essential
USA performance
• IEC 60825-1: 2007 - Safety of Laser Products
• ANSI/AAMI ES60601-1:2005 - Part1: Medical Electrical
Equipment General Requirements for safety and essential EMC
performance
• IEC 60601-1-2: 2007 Medical Electrical Equipment -
Canada Electro-Magnetic Compatibility Requirements & Tests
• EN 60601-1-2: 2007 Medical Electrical Equipment -
• CAN/CSA C22.2 No. 60601-1:14 - Medical Electrical Electro-Magnetic Compatibility Requirements & Tests
Equipment – Part 1: General requirements for safety and
essential performance

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