Portfolio brochure
An illustrated reference to the six devices and their practical design differences.
Download PDF ↓A review pack your team can work with.
Start with the public evidence and product guides. Then request the current, model-specific regulatory and supplier documents needed for your institution’s decision.
Available now
Begin the review without waiting.
Clinical overview
The supplied research overview. Pair it with the updated, source-linked evidence register.
Download PDF ↓Controlled product guides
Full multilingual instructions and English quick starts, with supplied revision numbers.
Find model-specific guides →Model cross-reference: Crescendo 2 6908 · Poco 6903 · Legato 6914 · Molto 6915 · Tenuto 2 6909 · Tenuto Mini 6907. The Remote controller is model 6905.
Request for your review
Specify the model, market and decision.
Declarations, registration records, supplier forms and commercial agreements are handled through the professional team, rather than a public download bundle.
Clinical review
- Exact model and current product information
- Relevant source publications and evidence context
- Patient information and support route
Regulatory review
- Device status and model identifiers
- Current intended-use and labelling materials
- Quality or compliance documents applicable to the request
Procurement review
- Supplier identity and quotation
- Ordering, delivery, warranty and returns terms
- Facility-specific forms or supplier onboarding requirements
Make the request
specific.
Include your facility, exact models and quantities, destination country, procurement route, required documents and review deadline. Avoid including patient-identifiable information.
Request a document packet →