Nordic Research Accessories AB supplies CE-marked medical devices and laboratory accessories to research institutions, biotechnology companies, and consumer markets across the European Union.
CE-marked accessories from ISO 13485-certified manufacturers, distributed to professional and consumer markets across Europe.
All medical devices in our catalog originate from ISO 13485-certified facilities with valid CE marking. Sourcing partners are audited annually. We maintain Declarations of Conformity for every SKU and serial-traceable lot records.
Operations follow EU MDR 2017/745 distributor obligations under Article 14. Storage at controlled temperature, traceable transport, vigilance reporting per Article 87, and post-market surveillance integrated into operational workflow.
Direct-to-consumer through brand-operated storefronts, institutional accounts for laboratories and research organizations, and wholesale partnerships with downstream distributors. E-commerce platform launching Q3 2026.
EU MDR 2017/745
ISO 13485:2016
CE marked devices
Läkemedelsverket (SE)
For complete documentation of compliance procedures, vigilance system, and quality management, see our Compliance statement.
For laboratory procurement, custom order quantities, or regulatory documentation requests, contact our team directly.