Cleaning, Pretreatment to Meet Medical Specs SO 13485 or FDA 21CFR820

摘要

A. All over the world, companies producing implants, surgical instruments, medical tubes, electromedical equipment, optical and dental equipment and medical fixtures - and even companies producing prefabricated parts and moldings for the medical device industry - must produce in accordance with quality systems such as ISO 13485 or FDA 21CFR820.