Quality ManagementWhy Choose Yasojima
ISO9001
Certificate of Registration
Yasojima Proceed Co., Ltd. emphasizes social responsibility based on strategic organizational management. To achieve a sustainable future, we optimize processes and continuously improve throughout the organization. With the aim of contributing to the development of society while providing products that exceed customer expectations, we adhere to the following:
- We will gain trust and customer satisfaction by accurately grasping customer requirements and providing products that exceed their expectations.
- We set quality goals and regularly evaluate and review achievements.
- We understand and comply with all relevant legal and regulatory requirements.
- All employees understand and adhere to all quality policies.
- We regularly review our quality policy for continuous improvement of our quality management system;
Certificate of Registration
- Registration Date: May 13, 2014
- Registration Certification number: 50263
- Registration Agency: NQA (UKAS accredited)
- Scope of Application: Design, development, and manufacture of synthetic resin parts for semiconductor / FPD manufacturing equipment and precision equipment.
- Registration Business Scope: Headquarters, Sendai Branch, Tokyo Branch, Yokohama Branch, Nagoya Branch, Shiga Branch, Osaka Branch, Kobe Branch, Fukuoka Branch, Technology Center, Sendai Factory, Shiga Factory, Osaka Factory, Kyushu Factory, Kobe Factory.
Certificate of Registration
ISO13485
Quality Policy
Yasojima Proseed Co., Ltd. provides high-quality products with the highest priority on safety through the manufacture of medical devices based on legal and regulatory requirements. In addition, with the aim of living up to the trust of society and continuously improving the effectiveness of our quality management system, we adhere to the following:
- We will continuously improve and maintain our quality management system to ensure that it functions effectively in accordance with standard requirements and other applicable regulatory requirements.
- We set quality goals and regularly evaluate and review achievements.
- All employees understand and adhere to all quality policies.
- We regularly review our quality policy for continuous improvement of our quality management system;
BS EN ISO 13485:2016
- Registration Date: March 10, 2009
- Registration Certification number: 25305
- Registration Agency: NQA (UKAS accredited)
- 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
Medical Device Manufacturing Permit
Permission Number：04BZ200007
- Name: Yasoshima Proceed Co., Ltd.
- Factory: Sendai Factory
- Location of the Factory: 2-1-4 Kamisakuragi, Tomiya City, Miyagi
- Permit Classification: Medical devices in general.
- Validity Period: November 7, 2018 to November 6, 2035
Certificate of Registration
MSJ4000 / Mitsubishi Heavy Industries, Ltd. Nagoya Aerospace Systems Works
MSJ4000
- Approval number: MHIY-3027
- Facilities: Shiga Factory, Sendai Factory, Kyushu Factory, Nagoya Branch, Technology Center.
- Applicable Specifications: MSJ4000
- Basic Requirements: AS / EN / JIS Q 9100: 2016
- Scope of Application: Manufacture and sale of synthetic resin parts for aircraft.
- Initial Approval Date: July 15, 2009
Certificate of Registration