Sil-Pro

Sil-Pro Medical Device Manufacturing Sil-Pro Medical Device Manufacturing

Certifications

Sil-Pro operates a Quality Management System which complies with the requirements of ISO 13485:2003 for the following scope: manufacture of components, subassemblies and final assemblies using in-house tooling, machining and automation, thermoplastic molding, silicone molding and silicone extrusions primarily for medical device applications and other high-tech industries.

Sil-Pro operates a Quality Management System which complies with the requirements of ISO 9001:2008 for the following scope: manufacture of silicone parts, subassemblies and assemblies using transfer molding, liquid injection molding, extrusion and bonding for medical, food, and electronics industries.

ISO-Large

Download ISO 9001:2008
Download ISO 13485:2003