SUBMED supplies sterile surgical packs, drapes, gowns and procedure kits to hospitals and clinics across Europe. Our products are developed and manufactured under a quality management system and are supplied with the technical documentation, labelling and traceability that healthcare providers and procurement teams require. CE marking is applied where required under Regulation (EU) 2017/745 (MDR), and copies of certificates and declarations of conformity are available on request.
For the United States, SUBMED has met FDA requirements, including establishment registration, device listing and Quality System Regulation compliance for labelling, packaging and sterilisation, and can provide FDA export certificates on request.
