The meaning of sterilization is to remove bacteria and other microorganisms stored in medical devices, transform non-sterile products into sterile products, ensure the safety and harmlessness of medical devices, and maximize the creation of a sterile environment. The sterilization verification of medical devices is of great significance to the safety of medical process.
At present, Pony Testing Group has set up four major medical device key laboratories in Beijing, Shanghai, Qingdao and Wuhan, covering various professional fields such as active and passive medical device products safety, EMC, environmental testing, medical software, biocompatibility, packaging and transportation, chemical characterization, pharmaceutical packaging materials, clean workshop and large animal testing. With many advanced instruments and equipment, and passed the CMA/CNAS qualification recognition, the test is professional and efficient, the data is accurate, the test report has international credibility, and it is also the third party big health service head enterprise. The test reports issued meet the requirements of medical device domestic registration, CE registration, FDA registration and other regulations, and can provide medical device enterprises with the whole process technical support from raw material research and development to the terminal product listing.

Test product

Medical equipment, cosmetics, disposable sanitary products, etc.

Test item

Radiation sterilization dose setting, ethylene oxide sterilization residue (EO/ECH), cleaning sterilization verification