Strouse, an industry leading adhesive tape converter and custom manufacturer is proud to announce its medical device establishment registration with the United States Food and Drug Administration (FDA). The registration builds on Strouse’s wide range of adhesive tape converting capabilities and allows for deeper penetration into medical device projects and the overall medical and healthcare market.
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Topics: Medical Strouse News Quality Assurance
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Strouse is proud to announce that it has earned ISO 13485:2003 registration from SAI Global. The standard was designed to be used by organizations involved in the design, production, installation, and servicing of medical devices. As the healthcare and medical markets continue to solve more complex challenges, the ISO 13485 standard aims to serve as a framework for regulatory requirements through every step of a product’s life cycle.