EUDAMED Compliance Specialist for Medical Device Importers

Qiyuan Technical Services helps European importers navigate their EUDAMED obligations — from UDI-DI status checks to manufacturer follow-up and tender compliance reports. Our Q+ platform is built around MDR / IVDR requirements, giving importers the visibility and documentation they need to stay market-ready.
 

Win European hospital tenders EUDAMED compliance evidence is becoming a requirement in EU public procurement. Qiyuan delivers certified UDI-DI status reports and tender submission packages — signed, dated, and ready to attach to your dossier. No last-minute screenshots, no manual checking under deadline pressure.
 

One partner across your full supply chain Whether your suppliers are based in China or elsewhere, we contact them directly with a structured compliance brief — in Chinese when needed, in English otherwise. You stay focused on your business while we track progress weekly until your portfolio is compliant.
 

Keywords · EUDAMED · UDI-DI · MDR · IVDR · medical device compliance · EU registration · PRRC · notified body · hospital tender · importer obligations · MDR Art. 13 · UDI-DI status report · tender submission package · EUDAMED compliance evidence · European importer · distributor compliance · Qiyuan Technical Services · Q+

About Qiyuan Technical Services Qiyuan Technical Services is a medical device regulatory compliance specialist serving European importers and distributors. With deep expertise in EUDAMED, MDR, and IVDR, we help importers verify their portfolio's compliance status, engage their suppliers, and produce the documentation that tenders require. Contact us: qiyuan-ts.com