Certification Symbol DescriptionTÜV RheinlandIndicates the device or product complies with applicable technical and safety requirementsfollowing testing by Technischer Überwachungs-Verein, (Technical Inspections Organization).1.5.14.3 Installation and ConnectionIf the installation of this equipment in the USA will use 240V rather than 120V, the source must be acenter-tapped, 240V, single-phase circuit.Contact GE Healthcare for information before connecting any devices to this equipment that are notrecommended in this manual or the supplies and accessories reference guide for this system.1.5.14.4 TrainingThis manual is intended as a supplement to, not a substitute for, thorough product training. If youhave not received training on the use of the system, you should request training assistance from GEHealthcare.To see available training, go to the GE Healthcare training Web site (http://www.gehealthcare.com/training). Select Education>Product Education-Technical>Diagnostic Cardiology.For more self-paced course offerings, tools, and reference guides you may find useful, please visit the GEHealthcare Education Store at http://www.gehealthcare.com/educationstore.1.6 Equipment IdentificationEvery GE Healthcare product has a product label that identifies the product name, part number,manufacturing information, and unique serial number. This information is required when contacting GEHealthcare for support.1.6.1 Product LabelThe product label is laid out in the following format. Depending on the product, the label may varyslightly in format, but it contains the same information.Item Description1 Product description2 Date of manufacture in YYYY-MM-DD format3 Product bar codeContinues on the next pageOperator Manual 1.6 Equipment Identification2053535-002 Revision T MAC 2000 ECG Analysis System 27/198