ISO 18250-7 Medical Devices - Connectors for Reservoir Delivery Systems for Healthcare Applications - Part 7: Connectors for Intravascular Infusion

EUROLAB, with its state-of-the-art accredited laboratories and expert team, provides precise and fast testing services within the scope of ISO 18250-7 testing. This standard specifies interface dimensions and requirements for the design and functional performance of connectors intended for use to connect intravascular infusion sets to intravascular infusion reservoirs.

This standard does not specify dimensions and requirements for medical devices or accessories that use these connectors. Such requirements are given in international standards specifically for certain medical devices or accessories.

Medical devices that may use intravascular reservoir connectors include:

• Administration ports on IV fluid reservoirs and matching spikes of IV administration-intravascular infusion sets-lines, such as IV bags-containers and spike inlet ends of IV sets;
• Devices intended to be connected in series between the administration port of IV fluid reservoirs and the mating spikes of IV administration/delivery lines;
• Syringes and syringe IV sets using Luer connectors.

Manufacturers are encouraged to include the connectors specified in this standard in their intravascular infusion medical devices or accessories, even if they are not currently required by certain medical device standards. When certain medical device standards are revised, it is expected that requirements for reservoir connectors as specified in ISO 18250 will be included.

EUROLAB assists manufacturers with ISO 18250-7 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.