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Power Systems User's Guide Appendix C: Power System Specifications
1110227 Revision 2
November 2006 43
Appendix C: Power System Specifications
Storage Requirements
• The unit must be fully charged prior to storing.
• The electronic enclosure on the 26 Amp-Hour unit must be unplugged from AC power
source and separated from battery enclosure.
• The Power Output Disconnect Switch on the 35 Amp-Hour unit must be set to the
OFF position.
Classifications
• Class 1, Internally Powered
• Degree of Protection against Harmful Ingress of Water, IPX0
• EQUIPMENT not suitable for use in the presence of a FLAMMABLE ANAESTHETIC
MIXTURE WITH AIR or WITH OXYGEN OR NITROUS OXIDE.
Environmental Specifications
• Operating Temperature: -25°C to 40°C
• Relative Humidity: 5 – 95% non-condensing
Warranty
• Product Warranty: 1 year limited warranty
• See
http://www.stingermedical.com for full warranty details
Approvals
ETL/cETL Listing for North America
• UL 60601-1 - UL Standard for Safety Medical Electrical Equipment, Part 1:
General Requirements for Safety First Edition
• CSA C22.2 NO 601.1-M90 - Issue:1990/01/11 (R2001) Medical Electrical
Equipment - Part 1: General Requirements for Safety General Instruction No 1;
Supplement 1; 1994; Amendment 2 - February 1998 (R1997)
Medical Device Directive 93/42/EEC - European Union (EU) Testing and Report Services
• CENELEC EN 60601-1 - Medical Electrical Equipment Part 1: General
Requirements for Safety Incorporates Corrigendum July 1994; Includes
Amendments A1: 1993, A11: 1993, A12: 1993, A2: 1995 and A13: 1996; IEC
601-1: 1988 + A1: 1991 + A2: 1995 + Corrigendum 1995, Modified
• IEC 60601-1-2 (2001-09) - Medical Electrical Equipment - Part 1-2: General
Requirements for Safety - Collateral Standard: Electromagnetic Compatibility -
Requirements and Tests Second Edition
CB Scheme Report and Certificate
• IEC 60601-1 - Medical Electrical Equipment Part 1: General Requirements for
Safety Second Edition