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What is CE Certification?
CE certification is the process of verifying that a product meets the essential health and safety requirements set by the European Union. The CE mark is proof that a product has been assessed and meets these requirements. Products carrying the CE mark can be sold in all EU member states. The CE Marking Directive sets out the specific requirements products must meet in order to be CE certified. These requirements cover a wide range of issues, including product safety, electromagnetic compatibility, environmental impact, and health and safety.

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The Intravascular Ultrasound (IVUS) Devices Market is experiencing significant growth due to technological advancements, increased prevalence of cardiovascular diseases, and expanding applications in both clinical practice and research. The market is expected to continue evolving as it addresses the healthcare needs of an aging global population.

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