The Regulatory Compliance Mark (RCM) is a trademark owned by the Australian electrical regulatory authorities (Regulatory Authorities, RA) and the Australian Communications and Media Authority (ACMA).
1. Household appliances (e.g., washing machines, refrigerators)
2. Electronic devices (e.g., computers, phones)
3. Electrical lighting (e.g., lamps, light bulbs)
4. Power tools (e.g., drills, lawnmowers)
5. Telecommunications equipment (e.g., routers, televisions)
6. Medical devices (e.g., ECG machines, X-ray machines)
7. Laboratory equipment (e.g., spectrometers, meters)
8. Electrical accessories (e.g., power outlets, extension cords)
9. Industrial equipment (e.g., production machinery, robots)
10. Renewable energy products (e.g., photovoltaic panels, EV chargers)
Based on the risk level that electrical equipment poses to people and property (as defined in relevant standards), electrical equipment is categorized into:
Level 1 (Low risk)– Requires EMC report
Level 2 (Medium risk)– Requires EMC report and safety report
Level 3 (High risk)– Requires EMC report, saa certification, and EESS registration
The specific category of a company’s product must be evaluated by a laboratory to determine its classification and applicable testing standards.
1. All suppliers responsible for selling in-scope electrical equipment must be a legal entity in Australia or New Zealand (including foreign companies with commercial registration in Australia or New Zealand) and must be registered as a Responsible Supplier in the national database.
2. All certificates used as evidence of compliance must have appropriate details recorded in the national database.
3. All in-scope electrical equipment must bear the Regulatory Compliance Mark (RCM).
4. Responsible suppliers must declare that all in-scope electrical equipment they supply is electrically safe.
5. Failure of a Responsible Supplier to fulfill obligations under the EESS may result in severe penalties and possible deregistration.
1. Product category evaluation by JJR Laboratory in China
2. Sample submission for testing
3. Testing and certification according to the applicable category requirements
4. Laboratory provides test results
5. Rectification (if necessary) until tests are passed
6. Submission of original reports and certificates for RCM application and registration
7. Successful registration and issuance of RCM documentation
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