Quality
 
SteriPack's commitment to quality is unmatched in our industry. SteriPack was the first designer/manufacturer to be certified by the FDA in April 1997 for processing instrument case/tray systems in autoclave manufacturer's standard cycles. This eliminates extending standard sterilization cycles and the burden and costs placed on hospital sterilization processing departments to add extra personnel for second shifts to accommodate delays in processing daily work loads due to extended cycles.

SteriPack has achieved ISO 9001-2000 and ISO 13485-2003 certifications to ensure the highest quality products for our customers.