ISO 18250-3 Connectors for Medical Devices, Healthcare Applications, Reservoir Distribution Systems - Part 3: Enteral Applications

EUROLAB, with its state-of-the-art accredited laboratories and expert team, provides precise and fast testing services within the scope of ISO 18250-3 testing. This standard specifies dimensions and requirements for the design and functional performance of connectors intended for use in enteral reservoirs.

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

Manufacturers are encouraged to include the connectors specified in this document in enteral 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.

This standard does not apply to screw and crown mushroom caps and necks as there are no medical device specific connectors. They belong more to the food and beverage packaging field, although often enteral delivery sets need to connect with them.

EUROLAB assists manufacturers with ISO 18250-3 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.