Infusion Pumps in Wisconsin

Bemis Manufacturing Company is a family-owned medical device plastics molding and injection molding manufacturer headquartered in Sheboygan Falls, Wisconsin. Since 1932, the company has produced quality toilet seats under the Bemis, Mayfair, and Bio Bidet brands for consumer and professional markets. The Healthcare Products division specializes in medical device plastic molding, manufacturing suction canisters, waste containers (including the proprietary Quick-Drain™ system), and specialty medical waste collection devices. The company's Contract Group provides custom plastic injection molding services across multiple industrial sectors including agricultural, construction, recreational products, lawn and garden, heavy truck, furniture, and healthcare markets. Bemis also owns Kelch, established in 1956, which supplies fluid and air management solutions including caps, gauges, sensors, tank accessories, and custom fitments. The company operates with state-of-the-art injection molding technology and emphasizes regulatory knowledge, engineering expertise, and responsive customer service. Manufacturing capabilities include custom plastic molding for medical applications requiring adherence to medical device standards.

QMD is a full-service medical device contract manufacturer specializing in silicone and elastomeric components, precision subassemblies, and finished device manufacturing. The company serves original equipment manufacturers (OEMs) across cardiology, critical care, infusion therapy, and surgical/respiratory applications. QMD's core capabilities include end-to-end manufacturing from component design through finished-device assembly, custom molded silicone and polyisoprene components (tubing, seals, valves, stoppers, duckbills), device assembly in ISO Class 7 & 8 cleanrooms, and packaging/sterilization services (ETO and gamma sterilization). Product portfolio includes coronary and peripheral vascular catheters (PTCA, PTA, aspiration), urinary catheters, enteral feeding tubes, central venous catheters, invasive blood pressure monitoring systems, chest and wound drainage products, and custom fluid management/respiratory/surgical subassemblies. The company holds FDA approvals, CE marking, 510(k) clearances, and Canadian regulatory licenses. Manufacturing capabilities span component-level customization through validated NPI processes, with private labeling and branded product transformation services. QMD operates Class 7 & 8 ISO-certified assembly facilities and provides comprehensive engineering and regulatory support to facilitate market entry for medical devices.