CERTIFIED AND COMPLIANT
All products in this catalogue are CE marked and manufactured under ISO 13485. Our operations fully comply with the European Medical Device Regulation (MDR 2017/745), which sets strict requirements for product safety, clinical performance, and post-market oversight.
For distributors, hospitals, and procurement professionals, this means:
Full technical documentation to support tenders, registration, and approval processes. Reduced administrative delays during audits and evaluations. Lower supplier risk, with clearly defined accountability. Confidence that products are manufactured and monitored with patient safety as a central focus.
This level of compliance is more than a regulatory requirement. It is a safeguard for healthcare providers and a quality signal for those seeking reliable long-term partners.
Aprikos Medical oers a broad medical furniture portfolio, adaptable configurations and short lead times. CERTIFIED AND COMPLIANT
If you do not find a product in this catalogue that fully meets your requirements, we encourage you to contact us. In many cases, we can propose suitable alternatives or support tailored configurations that align with your needs.
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