Safety, Technical Description, and Accuracy
10-20 ACUSON Cypress™ Operator’s Manual
Technical Description and Accuracy
Specifications
Model
ACUSON Cypress™
Manufacturer
Siemens Medical Solutions USA, Inc.
1230 Shorebird Way
Mountain View, CA 94043
650-969-9112
Electrical Power Requirements
Input Voltage: 100—120 V/220—240 V
Frequency: 50/60 Hz
Current: 1.2/0.6 A
Fuse Rating: 2.5A SB-250 V
Fuse Type: 3AG or 5 x 20 mm
Classifications
The Cypress is classified under IEC 60601-1, CSA 601.1, and UL2601-1 as:
1. Class I protection against electrical shock.
2. For continuous mode of operation.
3. Equipment not suitable for use in the presence of flammable anesthetic
mixture with air or oxygen or nitrous oxide.
4. Ordinary equipment without protection against ingress of water.
The Cypress system has two applied parts:
1. The transducer is classified as a type BF applied part.
2. The ECG cable is classified as a defibrillation-proof type CF applied part.
Environmental Conditions
Operating:
Temperature: 10°C to 40°C (50°F to 104°F)
Humidity (RH): 10% to 80%
Pressure: 700hPa to 1060 hPa (20.7 inHg to 31.3 inHg)
Transportation and Storage:
Temperature: –20°C to 60°C (–40°F to 158°F)
Humidity (RH): 10% to 90%, Non-condensing
Pressure: 500hPa to 1060 hPa (14.8 inHg to 31.3 inHg)
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