The ISO 11137 standard is an international standard specifying methods for sterilizing medical products using ionizing radiation, such as gamma and X-ray. The ISO 11137-FUTENG certification confirms that the product meets stringent requirements for the elimination of microorganisms, ensuring safe and effective use. This guarantees that the sterilization process is controlled, conducted in accordance with best practices, and that the product is safe and ready for medical use.

The ISO 13485 standard defines international guidelines for quality management systems in medical production, encompassing the design, production, and service of medical devices. It is a hallmark of the highest quality and safety in the medical industry. The ISO 13485-FUTENG certification confirms that processes related to medical products, including sterilization using ionizing radiation, comply with international standards. This ensures credibility and guarantees the highest level of safety for organizations and products certified under this mark.

ISO certification is an international recognition for companies that adhere to the highest quality standards. It ensures that suppliers adhere to best practices and deliver high-quality products. Possessing this certification demonstrates the maturity and professionalism of an organization and minimizes the risk of customer dissatisfaction. ISO certification guarantees the quality of our products and confirms the reliability and trust placed in us by our business partners and consumers. Thanks to this certification, our customers can be assured that they are receiving laboratory products manufactured to the highest applicable standards.

In vitro diagnostic (IVD) medical products are marked in accordance with European regulations that guarantee their safety, quality, and effectiveness. This marking confirms that the product meets the requirements necessary for placing it on the European market. The CE mark, awarded by authorized assessment bodies, known as notified bodies, is the result of independent assessments and tests of medical products. These bodies are responsible for verifying that a given product complies with EU standards and regulations for medical devices, which is crucial for ensuring the safety and effectiveness of products available to consumers on the market.