| | U.S.A. | SWEDEN | NORWAY | GERMANY |
| COMPANY | Solid Waste Transfer & | ELKRETSEN | Elektronikkretur AS | vfw AG |
| Recycling Inc |
| | | | |
| | | ELKRETSEN Box | | Max Plank Strasse |
| | | 1357, 111 83 | |
| | 442 Frelinghuysen Ave | 6454 Etterstad 0602 Oslo | 42 |
| ADDRESS | Stockholm |
| Newark, NJ 07114 | Fyrstikkalln 3B | 50858 Collogne |
| | Barnhusgatan 3, 4 |
| | | | Germany |
| | | tr. | |
| | | | |
| TELEPHONE 973-565-0181 | 08-545 212 90 | 23 06 07 40 | 49 0 2234 9587 - 0 |
| FAX | Fax: 973-565-9485 | 08-545 212 99 | 23 06 07 41 | |
E-noneinfo@el-kretsen.se adm@elektronikkretur.no vfw.info@vfw-ag.de
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Medical Requirement
Classifications:
In accordance with UL 2601-1/IEC 60601-1, the product is cssified as Continuous duty Class I equipment, which is not protected against ingress of liquids. The product is not suitable for use in the presence of a flammable anaesthetic mixture with air or with oxygen or nitrous oxide.
EMC
This equipment has been tested and found to comply with the limits for medical devices to the IEC 601-1-2:1994. These 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 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 does cause harmful interference to other devices, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:
zReorient or relocate the receiving device.
zIncrease the separation between the equipment.
zConnect the equipment into an outlet on a circuit different from that to which the other device(s) are connected.
zConsult the manufacturer or field service technician for help.
Video In / RS 232 / Video Out
Accessories equipment connected to the analog and digital interfaces must be certified to the respective IEC standards (i.e. IEC 950 for data processing equipment and IEC 601-1 for medical equipment.) Furthermore all configurations shall comply with the system standard IEC 601-1-1. Everybody who connects additional equipment to the signal input part or signal output part configures a medical system, and is therefore, responsible that the system complies with the requirements of the system standard IEC 601-1-1. If in doubt, consult the technical services department or your local representative.
Transport and Storage Limitations:
Temperature Range of -40°C to +70°C
Relative Humidity of 10 -95%, non-condensing
*Bio-accumulative is defined as substances which accumulate within living organisms.
**Lead, Cadmium and Mercury are heavy metals which are Bio-accumulative.
