Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Navigate Evolving IEC 61000 Standards for Implantable Medical Devices such as Cochlear Implants, Defibrillators and more
To ensure patient safety, personal protection and continuous reliable operation, you must verify your implanted device’s compliance to safety, EMC, and product-specific standards related to its purpose and function. We test a wide range of equipment, including ISO 14708 series for implantable devices:
The electromagnetic environments experienced by active implantable medical devices are different from those encountered by common types of medical electrical equipment. Partner with Intertek to ensure compliance to these basic EMC standards:
|IEC 61000-4-3||RF Radiated Immunity|
|IEC 61000-4-8||Radiated Magnetic Immunity|
|IEC 61000-4-20||Radiated Emissions|
Intertek does not provide consulting services for management systems certification. Any consulting activities provided by Intertek are separate and independent from certification activities.
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