ISO 13485 Medical Devices Quality Management System

ISO 13485 Certification for Medical Devices Quality Management System serves as an important foundation for medical devices to meet relevant regulatory requirements in most countries, and also demonstrates your commitment to fulfilling customer requirements. 

Nevertheless, in most countries, compliance with ISO 13485 alone is insufficient for medical device manufacturers to satisfy all regulatory requirements; they also need corresponding regulatory certification certificates issued by regulatory authorized bodies.

However, medical device subcontractors, component manufacturers, service providers and medical device distributors generally only need to obtain an ISO 13485 certificate. Medical device certification applies equally to brand owners, small-scale manufacturers and multinational enterprises.

Application Conditions
  • Applicable to one or more phases of the medical device life cycle, including design and development, production, storage and distribution, installation or servicing of medical devices, and design and development or provision of associated activities (e.g. technical support). It can also be used by suppliers or external parties that provide products (including quality management system-related services) to such organizations;

  • The system shall have been operated for no less than three months;

  • Companies applying for ISO13485 certification registration shall maintain management system records covering a continuous period of at least 3 months, including complete records of internal audit and management review.


Application Materials
  • Contract;

  • Application Form;

  • Business License and Organization Code Certificate (verify within validity period);

  • Other valid qualification certificates (Production License, etc., where applicable);

  • Company Profile;

  • Organization Chart;

  • Product Process Flow Chart;

  • Product Instructions (where applicable, e.g. required for finished products);

  • List of applicable laws and regulations, including list of product standards (where applicable, e.g. required for finished products);

  • Recent national or industrial supervision and random inspection report on products/services (if available).

Relevant Standards
  • ISO 13485:2016 Medical devices — Quality management systems — Requirements for regulatory purposes

  • GB/T 42061-2022/ISO 13485:2016 Medical devices — Quality management systems — Requirements for regulatory purposes


Value & Benefits
  • Help eliminate technical barriers to international trade and serve as a passport to enter the international market;

  • Improve the management level of the organization;

  • Enhance business reputation;

  • Raise the capability to guarantee product quality;

  • Help strengthen enterprise competitiveness;

  • Improve the internal management of the organization.

Service Process
  • Application Submission

  • Preliminary Review

  • Formal Audit

  • Certificate Issuance

  • Surveillance

  • Recertification

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