For distribution partners
Bring individually dosed IHHT® to clinical practice.
Build your ReOxy® market with a clear clinical story, documented medical-device engineering and a plan for local implementation. Tell us about your territory, clinical network and service capability.
Partner portal
Build the right support for your market.
Discuss the materials, training, regulatory documents and service arrangements your market needs. Digital partner services are being developed; available support and responsibilities are agreed for each territory.
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Approved marketing materials
Request the current presentations, clinical summaries and event materials for your market. Use the released version and agree local adaptations with AiMediq.
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Regulatory documents
The regulatory pack for your territory, with dated document versions.
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Regional clinical studies
Research activities in your region, with the rules on how they may be discussed.
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Product knowledge and training
Discuss product knowledge, clinical communication and operator or service training for the roles on your team.
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Opportunities and follow-up
Discuss how opportunities will be recorded, assigned and followed up in your territory. Project protection and any transfer of contact details are defined in the applicable agreement.
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Service requests
Agree the service contact, escalation route and support arrangements for devices in your territory.
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Spare parts and consumables
Confirm the applicable accessories, spare parts, ordering route and delivery terms with the service team.
Become a partner
Apply to become a distribution partner
Tell us about your company, territory and clinical network so we can discuss a suitable next step.
What we look for
- Sales experienceSelling capital medical equipment to cardiology and rehabilitation, with access to cardiac rehabilitation clinics in your territory.
- Clinical competenceA clinical specialist on your team, or a plan to hire one.
- ServiceYour own engineers who complete technical certification, or an agreed service route.
- Quality managementA documented quality management system. Certification to ISO 13485 is an advantage.
- ComplianceAnti-bribery and sanctions screening, no conflicts of interest, and adherence to the MedTech Europe Code of Ethical Business Practice.
- Data protectionReadiness to sign a data protection agreement before any lead is transferred to you.
Responsibilities for your market
Partners work within the applicable regulatory and quality requirements for their market.
Discuss your role, territory, device documentation, traceability, storage, service and complaint-reporting arrangements with AiMediq before supply.
Communication rules in every agreement
- Approved materials onlyUse the current released materials supplied by AiMediq. Agree local adaptations and translations before use.
- Within the intended useNo promotion outside the intended use, no guarantees and no unsupported comparisons — in print, online and in conversation.
- Prepared for your roleAgree and complete the training required for your team’s roles before demonstrating, installing or supporting the device.
How it works
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Application
Send the form. We will review your request and contact you to discuss the next step.
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Introductory call
Mutual qualification: your territory, portfolio, coverage of cardiac rehabilitation and regulatory capability; our programme and the device.
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Non-disclosure agreement and due diligence
You review the regulatory pack for your country. We run compliance and sanctions checks.
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Agreement and portal access
Territory, commercial terms, distributor obligations, communication rules and a data protection agreement for lead transfer. The agreed materials and working arrangements form part of onboarding.
- Partner programme
- [email protected]
- Next step
- Your enquiry will be reviewed by the relevant team.
- Meet us at MEDICA 2026
- Book a meeting at our booth · 16–19 November 2026, Düsseldorf
Questions partners ask
Do you offer exclusivity?
Territory and any exclusivity are part of the individual agreement. We make no commitments on this page.
Is ReOxy® available in my country?
Availability varies by country.
Regulatory status and registration are confirmed for your territory during due diligence.
Do we create our own marketing materials?
You use materials approved by AiMediq. Local adaptations and translations are approved by AiMediq before use.
Can ReOxy® be offered outside clinics?
No.
For use in a clinical environment under professional supervision and according to a doctor's prescription.
Is there a demonstration device?
Discuss demonstration requirements and terms with AiMediq.