DS-AUG26-PG63_Layout 1 20/07/2026 16:17 Page 1


55thanniversary


medical & pharmaceutical


industry focus


why waterproof connectors suit


medical device demands


over long service lives. Connector solutions that combine environmental protection with dependable electrical performance can help support the continuous operation of these systems. Similarly, patient monitoring systems


Brad Cunningham, director of industrial


products at pei-genesis, explains how sealed connector technologies help medical device manufacturers maintain reliable performance


E


quipment used in operating theatres, intensive care units and diagnostic facilities is routinely exposed to cleaning agents,


moisture, vibration and frequent handling. Every component within these systems must therefore be capable of withstanding such conditions throughout the device’s operational life. Connectors are often among the most exposed


components in a medical device. But, repeated mating cycles during maintenance, the risk of fluid ingress and the need to maintain power and data transmission can all affect performance. Sealed connector solutions that combine environmental protection with long-term electrical performance are therefore essential.


durability & reliability According to the U.S. Food and Drug Administration (FDA), the ability of connected medical devices and systems to safely and effectively exchange information is becoming increasingly critical as healthcare technology becomes more interconnected. Reliable connectivity therefore plays a vital role in maintaining device performance throughout its operational life. Amphenol’s D38999 Series III was developed


for applications requiring exceptional durability and reliability, with the connector combining environmental sealing, secure locking mechanisms and high contact density in a compact design. The sealing capabilities of D38999 Series III


connectors help protect sensitive electronics from moisture, cleaning agents and other contaminants that may be encountered in healthcare environments. Meanwhile, robust coupling mechanisms help maintain secure connections in equipment that is frequently moved, serviced or subjected to vibration.


www.designsolutionsmag.co.uk


reliable connectivity In surgical systems, reliable connectivity is essential for maintaining power and signal transmission between critical subsystems. Whether supporting imaging equipment used during procedures or advanced robotic- assisted surgical platforms, sealed connectors help minimise the risk of performance issues caused by environmental exposure or connection degradation. When it comes to diagnostic imaging


equipment, devices may be moved between departments, exposed to frequent cleaning procedures and required to operate reliably


rely on uninterrupted data transmission to provide clinicians with accurate real-time information. In critical care environments, connectors must maintain signal integrity while withstanding routine use, cleaning and maintenance activities. Sealed connector technologies help ensure these systems continue operating as intended when dependable performance is most important.


Medical device innovation As medical devices become more sophisticated and interconnected, the demands placed on connectivity solutions will continue to grow. Selecting the right connector is therefore an important consideration during the design process, helping manufacturers balance performance, durability and environmental protection requirements. By offering access to proven interconnect


solutions from leading manufacturers such as Amphenol, PEI-Genesis helps medical device designers identify connector technologies suited to the demands of modern healthcare applications.


pei-genesis http://www.peigenesis.com


pressure control for medical technology


The European Medical Device Regulation (MDR), along with standards such as DIN EN ISO 10993, 15001, and 18562, is making the development, documentation, and approval processes for new medical devices increasingly complex. Kendrion's compact Pure Flow Pressure Regulator 48.3 enables manufacturers to accelerate qualification processes and reduce overall development times. Developed for precise control of medical gases, the


Pure Flow Regulator 48.3 is suitable for use in ventilators, analytical instruments, anaesthesia equipment and dental technology. The development process considered relevant medical standards and incorporated suitable materials for medical use. In addition to medical gases, the pressure regulator can also be used in fluid applications, such as in dialysis systems. The Pressure Regulator 48.3 is designed to assist


from the initial product development phase, through improvements to existing devices, and during the replacement of pressure regulators. The pressure regulator is designed for low- to


medium-flow rates and delivers precise pressure control with high repeatability.


Kendrion www.kendrion.com/en/ July/auGust 2026 design solutions 1971-2026 63


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