ISO 13485 certification validates that medical device manufacturers have established and maintain quality management systems compliant with international standards. This certification demonstrates organizational capability to design, produce, and deliver safe and effective medical devices. Essential...
Manufactured by
IMQ Certification (Shanghai) Co., Ltd.
China
IMQ is a major European one-stop testing and certification service center with 30 years of experience in medical device testing. The company holds ISO 17025 accreditation, CB Testing Laboratory certification, and is a Notified Body for EU MDR 2017/745 and IVDR 2017/746. IMQ is the only Italian organization recognized as an Auditing Organization for MDSAP, enabling medical device exports to the USA, Canada, Brazil, Japan, and Australia.
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