Enagic Australia operates as part of the global Enagic group, a manufacturer of water ionisation and filtration equipment. Compliance, certification, and third-party verification form a core part of Enagic s operational framework across manufacturing, quality management, environmental management, and product safety.
This page provides verifiable, reference-based documentation relating to Enagic s certifications, patents, inspections, and regulatory approvals. All certificates listed below are issued by recognised authorities or accredited organisations and relate to manufacturing, quality assurance, and product standards.
Enagic Australia operates as part of the global Enagic group, a manufacturer of water ionisation and filtration equipment. Compliance, certification and third-party verification are key components of operational governance across manufacturing, quality management, environmental management and product safety.
The items listed below reflect documentation displayed on this website, including certifications, patents, inspection reports and recognition records. Where applicable, these can be cross-checked with the issuing organisations.
Certification recognising Enagic as a medical device manufacturer under applicable regulatory frameworks. This type of certification typically relates to documented manufacturing controls, traceability, and quality system governance.
Click here to view the Certificate of Medical Device Manufacturer
Recognition as a Medical Device Marketing Authorisation Holder supports documented responsibility for regulatory compliance, technical documentation maintenance and applicable post-market oversight requirements.
Click here to view the Medical Device Marketing Authorisation Holder documentation
Quality Management Systems
ISO 9001 is an internationally recognised quality management standard. Certification indicates structured processes for consistent manufacturing, quality control and continual improvement.
Medical Device Quality Management
ISO 13485 is specific to medical device quality management. Certification generally requires documented controls across design, production, traceability and risk management.
Environmental Management Systems
ISO 14001 relates to environmental management systems. Certification indicates a formal framework for managing environmental impacts and supporting environmental compliance.
Documentation indicates evaluation by recognised certification bodies including the Water Quality Association (WQA), NSF/ANSI standards programmes, and CSA Group. These certifications typically relate to material safety, structural integrity, and performance testing under defined standards and protocols.
Click here to view the WQA, NSF/ANSI, and CSA certifications
The Kangen Water® name and related intellectual property are protected through registered patents and trademarks. Intellectual property documentation supports product identity and ownership of the relevant marks and/or inventions.
Click here to view the Kangen Water® patent and trademark documentation
Patent documentation indicates formal examination and grant by a patent authority. Patents describe the protected technical scope and confirm the novelty of the claimed invention at the time of grant.
Patent documentation for the Ukon soft capsule supports that the invention (such as a formulation and/or delivery method) has been registered under patent law within the issuing jurisdiction.
Documentation indicating endorsement recognition for the Leveluk® series. Endorsement records are recognition-based and should be read in the context of the issuing body s criteria and defined scope.
Endorsements do not imply medical outcomes or health claims.
Click here to view the Leveluk Series endorsement recognition
Documentation indicating endorsement recognition for Ukon products. Where relevant, refer to the issuing body s criteria to understand what is covered and what falls outside the scope of the recognition.
Endorsements do not imply medical outcomes or health claims.
Inspection report documentation relating to Enagic Kangen Rice. Inspection reports typically summarise evaluation methods, testing scope, and results recorded at the time of inspection.
Report documenting inspection and testing for non-radioactive contamination, according to the scope and parameters described in the report. This supports product safety recordkeeping and quality assurance documentation.
Click here to view the non-radioactive contamination inspection report
Recognition indicating participation in a corporate social responsibility or ethical business initiative. Refer to the issuing program s criteria for specific requirements, scope, and assessment framework.
The certificates and records referenced on this page are provided as documentation images and reports as displayed on this website. Where applicable, certification validity and scope can be verified through the issuing organisations or their public registers.
This page is intended for informational and compliance reference purposes only. Certifications and standards listed here relate to manufacturing systems, quality management, environmental management, inspection/testing documentation, and intellectual property records.
Nothing on this page should be interpreted as a medical claim, health claim, performance guarantee, or income claim.
To provide reference context for certifications, inspection reports, patents and recognition documents displayed on this website, and to support transparency around standards-based documentation.
Certification scope varies. A certificate may apply to a specific facility, product line, standard version, or jurisdiction. Always check the scope, dates and issuing body details on the document itself.
Open the certificate to review validity dates and certificate identifiers, then verify via the issuing organisation s registry or verification process where available.
