Remarketing & Disposal
Equipment that is safe and still usable, but has fallen out of line with your requirements or minimum spec (perhaps following an ARP or ESP
We have rigorous measures in place to ensure compliance when re-marketing medical devices.
All equipment flagged for re-marketing is checked and decontaminated prior to removal from your site. As always, a full audit trail is made available by recording all work on HEMS. Any labels or client information are removed and destroyed.
Any equipment retaining patient data will be completely wiped and certified via Blancco.
Once equipment has been prepared for re-marketing, we then manage a fully auditable re-sale process, working with our commercial partners.