Product Specifications
Appendix C
Peut être utilisé dans des gaines transportant de l’air traité, conformément à la section 300-22(c) du National Electrical Code et aux articles 2-128, 12-010(3) et 12-100 du Code Canadien de l’électricité, Première partie, CSA C22.1.
EMC Compliance and Warning Statement
This equipment has been tested and found to comply with the limits of the standard for medical devices, IEC 60601-1-2:2001. The unit also complies with the requirements of EN 60601-1-2:1998, providing the presumption of compliance to the European Union’s Medical Device Directive 93/42/EEC. The limits are designed to provide reasonable protection against harmful interference in a typical medical installation. This equipment generates, uses and can radiate radio frequency energy, and, if not installed and used in accordance with the manufacturer’s instructions may cause harmful interference to other devices in the vicinity. However, there is no guarantee that interference will not occur in a particular installation. If this equipment causes interference with other devices, which may be determined by turning the equipment off and on, the user is encouraged to try and correct the interference by one or more of the following measures:
Reorient or relocate the device receiving the interference.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit different from that to which the other device(s) are connected.
Consult the manufacturer or field service technician for help.
44 Aruba AP 60/61 | 0500160 |
Installation Guide | December 2005 |