Quality is the foundation of Perma Pure’s operations. The company has been ISO 9001 registered since 2005 and has recently expanded its certifications, achieving ISO 13485:2003 status. This speciality registration sets out further rigorous requirements for the manufacture of medical devices and is in addition to Perma Pure’s registration with the US FDA as a Class 2 Medical Device manufacturer.
Select products are also CE certified and have Class 1 Division 1 and Class 1 Division 2 designations for hazardous area use. The company recently expanded its industrial offerings to include ATEX-rated systems for use in refineries and chemical plants.