IDENTIFY
Design a medical device to replace manual user operation compatible with ISO Class 5 100 clean room standards. Provide FDA documentation support for user instruction, fabrication, and assembly instructions.
DEFINE
Concept design exploration for mechanical systems to achieve an identified and consistent compression force.
REALIZE
Designed and engineered fully pneumatic drive squeeze system that included robustness, safety, serviceability and clean room compliance. The new device increased product throughput and reduced inconsistencies across multiple users.