Product Announcement from UFP Technologies, Inc.

Clean Room Manufacturing Services-Image

Since attaining ISO 13485:2003 certification in Glendale Heights in 2011, UFP Technologies has made significant investments within this facility to better service its customers in the medical industry. An ISO Class 8 (Class 100,000) clean room was constructed which qualifies the facility to produce up to Class III medical devices. New production machinery was installed within the clean room to manufacture custom components, products, and packaging from medical-grade foams and thermoplastic polyurethanes (TPU). The new capabilities, which include RF welding, high speed die cutting, and heat sealing, increase UFP Technologies’ manufacturing output by multiple-millions of parts per week.

“Investing in our medical manufacturing capabilities was vital to support the growing demands of our customers,” says Michael Zumpano, General Manager of the Glendale Heights facility. “Our facility is equipped to fabricate the latest medical-grade foams, films, and other specialty materials that we have access to from our broad supply base.”

The recent addition of advanced processing capabilities at Glendale Heights builds upon UFP Technologies’ strong presence as a valued manufacturing partner to medical device OEMs. Seven of its eleven manufacturing facilities are ISO 13485:2003 certified which house multiple ISO Class 8 (Class 100,000) and ISO Class 7 (Class 10,000) clean room facilities.

 
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