Technical Specifications
Progressa® Bed Instructions for Use (171528 REV 9) 93
Classification and Standards
The Progressa® Bed is designed and manufactured according to the following equipment classifications
and standards:
Electromagnetic Emissions Guidance
Caution—This device meets all requirements for electromagnetic compatibility per IEC 60601-1-2. It is
unlikely that the user will encounter problems with this device because of inadequate electromagnetic
immunity. However, electromagnetic immunity is always relative, and standards are based on
anticipated environments of use. If the user observes unusual device behavior, particularly if such
behavior is intermittent and associated with nearby use of radio or TV transmitters, cell phones, or
electro-surgical equipment, this could be an indication of electromagnetic-interference. If such
behavior occurs, the user should try to move the interfering equipment further from this device.
Warning—The P7500 should not be used adjacent to or stacked with other electrical equipment. If
adjacent or stacked use is necessary, observe the P7500 and the other electrical equipment to make
sure they operate as intended.
Make sure the P7500 operates correctly when it is used near other electronic devices. Portable and
mobile radio frequency (RF) communications equipment can affect electrical equipment.
Warning—Portable RF communications equipment (including peripherals such as antenna cables and
external antennas) should be used no closer than 30 cm (12 inches) to any part of the Heart and
Respiration Rate Monitoring System powered by EarlySense, including cables specified by Hill-Rom®.
Otherwise, degradation of the performance of this equipment could result.
Technical and Quality Assurance Standards ANSI-AAMI ES 60601-1
EN & IEC 60601-1
EN & IEC 60601-1-6
EN & IEC 60601-2-52
EN & IEC 62304
EN & IEC 62366
CAN/CSA-C22.2 No. 60601-1
CAN/CSA-C22.2 No. 60601-2-52
Equipment Classification per EN 60601-1 Class I equipment, internally powered equipment
Degree of Protection Against Electric Shock Type B
Classification According to Directive 93/42/EEC Class Im
Class IIa for therapy and pulmonary surfaces
Degree of Protection Against Ingress of Water Ordinary Equipment - IPX4
Degree of Protection Against the Presence of
Flammable Anesthetic Mixtures
Not for use with flammable anaesthetics.
Mode of Operation (Bed Articulation) Continuous operation with intermittent loading,
2 minutes ON/18 minutes OFF
Sound Level <65dBA
Application Environments Environments-1, 2, 3, and 5 per EN and
IEC 60601-2-52
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