Workflow demo
Ask to see setup, room fit, interface use, accessory handling, and staff handoff.
Ask a laser and shockwave equipment demonstrator to identify the exact configuration, explain its current documented clinical scope, and show the workflow your intended operators need to evaluate. Record purchasing and implementation questions that require written follow-up before deciding which modality belongs in the clinic. Chattanooga Rehab is a rehabilitation equipment manufacturer serving professional clinics with LightForce laser and Intelect shockwave systems.

Ask to see setup, room fit, interface use, accessory handling, and staff handoff.
Ask how training, warranty, service requests, and replacement parts are handled.
Ask which configuration is being shown and what is included in the quote.
Start by asking for the system name, configuration, supplied handpiece, and accessories shown. Ask which items are included in the proposed package and which are optional or separately arranged. Record differences between demonstration equipment and the quote. A demonstration of one setup does not establish that the clinic will receive the same components or have the same operating conditions.
Ask the representative to identify current labeling and operating documents for each system. Official Chattanooga sources describe laser, radial pressure wave, and focused shockwave separately. Keep questions about clinical scope and contraindications tied to the exact device, with qualified clinical review where needed. Do not infer that a comparison demonstration makes those systems interchangeable or expands their indications. [1] [3] [4]
Invite the clinicians who would operate the equipment and ask them to bring the clinic's proposed workflow. Request a demonstration of the relevant controls, compatible application components, documented setup, and equipment-record responsibilities. Ask staff to distinguish what they observed from what still requires instruction or confirmation. Keep notes specific enough that another purchasing reviewer can understand why a question remains open.
Bring information about the receiving room, storage, access, and equipment movement. Ask which current installation or safety requirements must be reviewed before delivery and who supplies the relevant instructions. Review operator instruction arrangements separately from the sales demonstration. Do not assume a demonstration authorizes clinical use, establishes competence, or resolves every site-specific preparation requirement.
Identify the exact system and components demonstrated. Let intended operators evaluate their own workflow questions.

Use the same evaluation categories for each modality, but retain device-specific answers. Ask what staff must prepare, which supplied components they will handle, what records they will maintain, and how they request support. Record the context of any demonstrated task rather than presenting an observed example as a universal appointment duration. Clinical scheduling decisions require the clinic's own review, not an extrapolation from a sales session.
Ask for the source and limitations of any clinical, operational, or financial statement made during the appointment. A demonstration does not establish guaranteed patient results, increased demand, or a revenue forecast. Request evidence and current approved wording before using a statement in the clinic's service descriptions. Keep unanswered claims out of the purchasing rationale until the responsible reviewer has assessed them.
Request an itemized proposal identifying the system, included quantities, optional components, delivery scope, instruction, written coverage, and service contacts. Ask how the proposed configuration differs from the equipment shown. Record room preparation and separately arranged support as distinct tasks or expenses. Avoid filling missing prices or terms with assumptions based on another clinic's purchase.
Keep a follow-up register with the question, requested document, responsible contact, and expected response date. Separate confirmed observations from unresolved clinical, room, purchasing, and support conditions. Bring those records to the clinic's purchasing review before approving the order. Use the rehab equipment demo checklist to organize the appointment and the equipment quote checklist to evaluate the written proposal afterward.
| Review area | Information to confirm |
|---|---|
| Configuration questions | System shown, compatible components, included items and quote differences |
| Operator questions | Controls, documented setup, instruction scope and equipment records |
| Workflow questions | Actual room, handling responsibilities and unresolved preparation needs |
| Follow-up questions | Supporting documents, itemized scope, task owner and response date |
No. Compare each system against the clinic's documented clinical role, operator requirements, room conditions, and purchasing criteria rather than a universal ranking.
Ask the representative to identify the demonstrated configuration and document differences from the proposed system, included components, and optional accessories.
Record the question, responsible contact, requested document, and follow-up date. Keep unresolved conditions visible before purchasing approval.
Questions for clinics, rehab directors, chiropractors, sports medicine teams, and purchasing groups evaluating equipment.
Bring the clinic room plan, staff roles, intended service workflow, budget range, decision timeline, and questions about current device labeling. Identify who approves clinical fit and who approves spending. Ask for a demonstration built around that workflow so the team can evaluate the same configuration.
Ask staff to evaluate setup, control access, accessory changes, cleaning, storage, and movement between rooms under supervision. Record questions that cannot be answered during the demonstration. Request the current instructions and follow-up documentation before accepting an equipment recommendation.
Request exact model identification, part numbers, quantities, included and optional accessories, training scope, shipping, warranty, service contacts, and quote expiry. Distinguish confirmed terms from estimates. Compare the quote with the demonstrated configuration before purchasing.
Use the same clinic requirements for each proposal and compare documented configuration, labeling, training, support, and total purchase scope. Record missing information as unresolved rather than assigning an assumed value. Avoid inferring clinical superiority from power, price, or a longer feature list.
Include a clinician who will operate the device, the clinical lead, the purchasing decision-maker, and the administrator responsible for implementation. Add facilities or safety staff when room controls need review. Give each person specific questions so the decision includes operation and ownership requirements.
Collect the written quote, instructions, configuration list, training plan, and unresolved answers. Document clinical and purchasing acceptance separately. Assign room-preparation and staff-training tasks before confirming delivery so the final decision is based on evidence the team can review.
Ask the representative to itemize the rehabilitation equipment configuration and the parts or services needed for this project. Record included quantities, optional purchases, training, delivery assumptions, and written support terms. Have the purchasing and clinical leads compare that scope with the specific requirements above before approval.
Request current instructions for the exact model, accessory compatibility information, the accepted quote, and the applicable warranty or contract terms. Record the document version and market. Use these records to resolve unanswered questions rather than relying on an older brochure or a general sales statement.
Have the clinical lead approve device fit and operation, the administrator approve staffing and room readiness, and the purchasing lead approve the written cost and contract scope. Include a safety or facility reviewer where needed. Keep each approval tied to the proposed configuration.
Separate the equipment purchase from accessories, staff time, training, shipping, inspection, maintenance, and service. Request current prices for applicable items and identify unknown costs. Review these assumptions with the financial lead without turning an estimate into a guaranteed annual expense or return.
Use the current operating instructions to review setup, device controls, accessory identification, care, and issue reporting. Record completed instruction and questions requiring follow-up. The clinical lead should decide when operators are ready under the facility policy rather than assuming attendance at a sales demo is sufficient.
Use the demo link on this page and provide the clinic type, room plan, operators, purchase timeline, and this topic's unresolved questions. Ask for a demonstration of the proposed rehabilitation equipment configuration and written follow-up on quote scope, training, and service.
1. Chattanooga. Class IV laser therapy devices: indications, safety, training, and equipment selection. Laser device indications, operating context, and training questions.
2. Chattanooga. Shockwave therapy devices: US indications and device categories. The US indication statement and distinction between focused shockwave and radial pressure wave.
3. Chattanooga. Intelect RPW 2: US product documentation and instructions. RPW device and accessory documentation. Confirm the current instructions for the quoted model.
4. Chattanooga. Intelect Focus Shockwave: US product documentation and instructions. Focused-system documentation and compatible accessories. These are separate from RPW accessories.
Individual results may vary. Neither DJO Global, Inc. nor any of its subsidiaries dispense medical advice. The contents of this website do not constitute medical, legal, or any other type of professional advice. Rather, please consult your healthcare professional for information on the courses of treatment, if any, which may be appropriate for you.
Review the current US instructions for the exact equipment configuration before approving clinical use, accessories, room controls, or staff training. Manufacturer documentation supports product facts; clinical research addresses its stated study population and methods. A study does not extend a device indication. [1]
Intelect Focus Shockwave has a US indication for heel pain due to chronic proximal plantar fasciitis in adults with failed alternative conservative therapies for at least six months. Review radial pressure wave labeling independently; do not transfer a condition claim between systems. [2]