Molnlycke Terms of Service
These terms govern professional use of the Molnlycke product-information website and submission of business inquiries.
1. Scope of information
Content on this site is intended for clinicians, biomedical engineers, procurement teams, and clinical informatics professionals. Product availability, labeling, and regulatory status vary by device family and market. Confirm the current IFU and regional registration before procurement or clinical use.
2. No medical advice or outcome guarantees
Nothing on this website constitutes medical advice, diagnosis, or a guarantee of clinical outcomes. Monitoring performance depends on labeling, configuration, operator competency, patient condition, and site conditions. Do not interpret planning examples as guaranteed MTBF, MTTR, SpO2 accuracy, or uptime claims for every installation.
3. Regulatory language
Where a device follows a 510(k) pathway, describe it as FDA cleared, not FDA approved, unless a specific PMA pathway applies. CE statements refer to CE marked under MDR 2017/745 where applicable.
4. Intellectual property
Site text, layout, and branding elements are owned by Molnlycke or its licensors. You may not copy materials for commercial redistribution without written permission.
5. Inquiries
Professional inquiries submitted through forms may be routed to clinical, service, or regulatory teams. Do not submit protected health information.
6. Updates
We may update these terms as site functionality or legal requirements change. Continued use after updates constitutes acceptance of the revised terms.