ARTEC
Anesthesia system
Operating instruction
Version 1.2. Status 04.10/
Picture shows Artec with optional components
Table of contents
| 1 | GENERAL INFORMATION | 5 |
|---|---|---|
| 2 | TECHNICAL DESCRIPTION | 6 |
| 2.1 | Possible Expansion and Upgrading of the Unit | 6 |
| 2.2 | Scope of Use and Application | 8 |
| 3 | DESCRIPTION | 9 |
| 3.1 | Gasmixing unit 3 and 4 | 9 |
| 3.2 | O 2 - Ratiosystem (optional) | 10 |
| 3.3 | O 2 -Flush | 11 |
| 3.4 | AIR/N 2 OMode Switch | 11 |
| 3.5 | O 2 - supply deficiency signal | 11 |
| 3.6 | Nitrous Oxide Block | 11 |
| 3.7 | Vaporizer | 12 |
| 3.8 | Gas-cylinder Supply Component | 13 |
| 4 | CHANGEOVER MOUNTING ARM (OPTIONAL) | 14 |
| 4.1 | Top view | 14 |
| 4.2 | Front view | 15 |
| 4.3 | Rear view | 16 |
| 4.4 | Connecting the changeover mounting arm | 17 |
| 5 TESTING UNIT FUNCTIONS | 5 TESTING UNIT FUNCTIONS | 21 |
| 5.1 | Dosage valves of the Gas Mix Unit | 21 |
| 5.2 | O 2 -Flush | 21 |
| 5.3 | AIR / N OMode Switch | 21 |
Table Caption: This table of contents outlines a technical document detailing the components, functions, and testing procedures for a gas mixing unit, including optional accessories like a changeover mounting arm. It covers general information, technical descriptions, detailed component descriptions, and specific functional tests.
Operating Instructions Artec
| 6 GAS TYPE TEST AND TESTING SAFETY DEVICES | 6 GAS TYPE TEST AND TESTING SAFETY DEVICES | 23 |
|---|---|---|
| 6.1 | Testing Gas Type: | 23 |
| 6.3 | Testing the Vaporizer / Vaporizer holding rack | 24 |
| 7 | CLEANING AND CARE OF ANESTHESIA UNIT | 25 |
| 8 | TROUBLESHOOTING | 26 |
| 8.1 | ARTEC | 26 |
| 8.2 | Changeover mounting arm (if available) | 27 |
| 9 | TECHNICAL DATA | 29 |
| 10 | MAINTENANCE AND SERVICING | 31 |
| 10.1 Artec | 10.1 Artec | 31 |
| 10.2 Changeover mounting arm (if available) | 10.2 Changeover mounting arm (if available) | 31 |
Table Caption: This table appears to be an index or table of contents for a manual, detailing sections related to gas type testing, safety devices, cleaning, troubleshooting, technical data, and maintenance, with corresponding page numbers.
1 General Information
The Medical Equipment Regulations (MedGV), and the law on technical medical working materials (MPBetreibV) stipulate that the attention of the operator must be drawn to the following:
The operation of the Unit must be carried out only by qualified personnel. Exact knowledge and understanding of the Operating Instructions is a pre-conditioned for operation.
Use of the equipment is solely for that as stipulated in the Operating Instructions.
Inspections and servicing must be duly entered in the Logbook of the Unit. The Equipment must be inspected at regular intervals by qualified personnel only.
F.Stephan GmbH stipulates a half-yearly inspection and maintenance by one of its authorized Service Technicians.
Before each use of the unit, a complete function test of the unit must be carried out. In the case on medico.technical devices with electrical connection, the standards of particular VDE 0751 and IEC 601 must be closely complied with. According to these standards, such devices may only be set up and put into operation by the manufacturer or his expressedly authorized technician or dealership.
Unit equipped with a pressure reducer should undergo a basic overhaul at least every 5 years for
