The Australian RCM (Regulatory Compliance Mark) is the core mark for Australian market access, used to demonstrate that a product complies with relevant Australian regulations and standards. It applies to multiple product categories including electrical equipment, radio communication devices, and medical devices. Below is key information on RCM registration:

I. Core Function of the RCM

The RCM is the "passport" for products entering the Australian market, indicating that the product has met all applicable mandatory regulatory requirements (such as electrical safety, electromagnetic compatibility EMC, radio spectrum, etc.), replacing the former SAA mark (safety certification) and C-Tick mark (electromagnetic compatibility) as a single unified compliance mark.

II. Applicable Product Scope

Primarily covers:


III. Responsible Entity

A local Australian entity is required to take responsibility for the product's compliance declaration and use of the RCM mark, including:


IV. Core RCM Registration Process

  1. Identify applicable standards and regulations
    Based on the product category, clearly identify the mandatory standards that must be met (e.g., electrical equipment must comply with the AS/NZS 60950 series safety standards, EMC must comply with AS/NZS CISPR 22, etc.), as well as the corresponding regulatory authorities (e.g., electrical safety is regulated at the state level, radio equipment is regulated by the ACMA).
  2. Product testing and report
    Engage a NATA (National Association of Testing Authorities, Australia) or ILAC (International Laboratory Accreditation Cooperation) accredited laboratory to perform testing and issue a test report demonstrating compliance with the applicable standards. Testing shall cover safety, EMC, radio performance (if applicable), etc.
  3. Sign the Declaration of Conformity (DoC)
    The responsible entity (local importer / manufacturer) shall sign a Declaration of Conformity, declaring that the product complies with all applicable regulations and standards. The DoC must include product information, test report number, responsible entity details, etc., and serves as the core document for RCM compliance.
  4. Registration and filing (if applicable)
    • Certain high-risk products (e.g., radio equipment, medical devices) must be registered or filed with the corresponding regulatory authority (ACMA, TGA), by submitting the test report, DoC, and other documents;

    • General electrical equipment does not require additional registration; only the DoC and test report need to be retained for potential regulatory spot checks.

  5. Affix the RCM mark
    After completing the above steps, affix the RCM mark on the product or its packaging (the mark must bear the "RCM" text, clearly and permanently displayed) before the product may be sold in the Australian market.

V. Important Notes


For specific product RCM compliance details, it is advisable to consult a local Australian compliance organization or a professional testing laboratory to ensure alignment with the latest regulatory requirements.