MEDICALQuality Management System (QMS)

Certificate of Registration

Medical Device Manufacturing Permit

Permission Number:04BZ200007
Name:Yasoshima Proceed Co., Ltd.  
Factory:Sendai Factory
Permit Classification:Medical devices in general

Certificate of Registration

ISO 13485:2016

Registration Certification number:25305
Scope of Application:Manufacture of artificial joints, artificial bones, orthopedic surgical instruments, blood transfusion device parts, robot surgical instrument parts.
Registered Business Scope:Medical Division, Sendai Factory

Certificate of Registration

The United States Food and Drug Administration (FDA)

Registration Number:3013557690

Manufacturing Facilities