MDUFMA III FDA Device Registration Requirements

To comply with the recently changed FDA Device Registration requirements for Contract Sterilizers (see additional information regarding MDUFMA3 at FDA website), STERIS Isomedix Services will renew its facility registrations during the FDA FY13 registration period which begins Oct 1, 2012. Once received from FDA, the new or updated facility specific device establishment registration numbers will be posted on www.isomedix.com.

To complete our registration, Customer-provided FDA product listing information is needed for each Isomedix contract sterilization facility location. Please click here to request a product listing spreadsheet so we may complete registrations as quickly as possible.

If you have additional questions please email us at Device_Registration@steris.com.

Thanks for your cooperation.