Application planning
Connect accessories to intended use, staff comfort, and documentation.
Focused shockwave stand-off purchasing should start with the exact system and compatible part identification, kept separate from radial pressure wave transmitters. Confirm included options, fitting, inspection, care, storage, and replacement ordering before approving the quote. Chattanooga Rehab is a rehabilitation equipment manufacturer serving professional clinics with LightForce laser and Intelect shockwave systems.

Connect accessories to intended use, staff comfort, and documentation.
Ask what accessories are included, optional, or replaced over time.
Confirm the training, service, warranty, and communication path after install.
Request the stand-off names, part numbers, quantities, and compatibility for the focused system under consideration. Separate the package supplied with the device from optional or spare accessories. Chattanooga provides a specific listing for the short F-SW stand-off, which illustrates why the purchasing record should use an identifiable part rather than a general description such as shockwave pad. [4]
Have the representative identify the current US instructions that cover the proposed accessory and handpiece. If a quotation uses different wording from the product documentation, resolve it before ordering. Include any associated items in the written configuration. The clinic should not discover during delivery that a photograph showed an option that was not part of its purchased package.
The clinical lead should review the available options within the labeling and operating instructions for the focused system. This is an equipment-selection discussion, not a new indication for a condition. Do not select an accessory solely because an article discusses shockwave for a particular tendon or because a search result describes a depth of application. [3]
During the demonstration, ask the representative to identify the compatible stand-off options and show the documented attachment process. Have operators review handling and identification before discussing extra quantities. If the practice is also comparing RPW, keep the accessory inventories separate. A radial transmitter and a focused stand-off should not be treated as interchangeable purchasing items.
Use model-specific part identification. Review the accessory within current focused-system labeling.

Request the manufacturer instructions for inspection, care, storage, and replacement. Identify the staff who prepare the handpiece and who report a questionable part. The clinic needs a clear way to isolate an accessory when its condition or identity is uncertain. Do not substitute a general cleaning routine from another device for the procedure supplied for the quoted system.
Ask for current replacement prices, part numbers, ordering contacts, and availability expectations. Clarify accessory coverage separately from the main system warranty. If the practice decides to purchase a spare, record why it is needed and where it will be stored. No universal calendar interval or replacement count is supplied here; the device documentation and actual condition should govern that discussion.
Compare the delivered device and stand-offs with the accepted configuration and record the supplied part identification. Check that current operating documents and the agreed instruction resources are available. Have the clinical lead resolve missing or uncertain accessories before the system enters the approved workflow. Keep the accepted accessory list with the service records for later replacement orders.
A focused shockwave demo can address the practical details that a parts list cannot show: identification, fitting, removal, storage, and staff handoff. Bring those questions to the representative with the planned purchasing scope. The aim is a documented, usable accessory package for the chosen system rather than an expanded inventory without a defined purpose.
| Review area | Information to confirm |
|---|---|
| Compatibility | Focused system, handpiece, exact stand-off part |
| Quote inclusion | Supplied quantity, optional items, agreed package |
| Daily handling | Instructions, fitting, inspection, storage |
| Replacement | Part identification, ordering contact, written coverage |
Request the exact part number, compatible focused system and handpiece, quantity, and current documentation before adding the accessory to the quote.
Ask for current compatible-part prices and ordering contacts. Review spare quantities against the clinic workflow and documented inspection requirements.
Compare accessory identification and quantities with the accepted quote. Have operators review documented attachment, inspection, care, and storage before acceptance.
Use the shockwave maintenance-cost guide to budget for accessory ordering and service separately from the initial stand-off package.
Questions for clinics evaluating equipment fit, training, support, service, safety, and purchase timing.
Ask the supplier to list the compatible stand-offs by name and part number for the exact focused system. Identify included and optional items separately. Confirm the accessories in the current US documentation rather than assuming an international bundle contains the same parts.
Treat them as separate accessory categories. Request compatibility documentation for the exact device and handpiece. A purchasing list should identify focused-system stand-offs separately from radial pressure wave transmitters so a similar-looking accessory is not ordered for the wrong system.
Ask the clinician and representative to review the available options using the device instructions and its permitted use. Compare compatibility, handling, care, storage, and quote inclusion. Do not choose an accessory from a condition name or assume a depth specification establishes an indication.
Yes. Ask the representative to show attachment, removal, inspection, and the documented care procedure with the proposed handpiece. Include the staff who will prepare the system. Record where the accessories are stored and how the team will identify the correct part.
Request replacement part numbers, current prices, order contacts, and availability expectations in writing. Use the device documentation for inspection and replacement criteria. Confirm whether a replacement is covered or a separate expense rather than assuming accessories share the main system warranty.
Record the device model, handpiece, stand-off description, part number, included quantity, optional quantity, source of compatibility guidance, and replacement contact. Keep that list with the accepted quote so later orders do not depend on an informal accessory name.
Ask the representative to itemize the shockwave 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 shockwave equipment configuration and written follow-up on quote scope, training, and service.
1. Chattanooga. Shockwave therapy devices: US indications and device categories. The US indication statement and distinction between focused shockwave and radial pressure wave.
2. Chattanooga. Intelect RPW 2: US product documentation and instructions. RPW device and accessory documentation. Confirm the current instructions for the quoted model.
3. Chattanooga. Intelect Focus Shockwave: US product documentation and instructions. Focused-system documentation and compatible accessories. These are separate from RPW accessories.
4. Chattanooga. F-SW Stand-off I (Short), SKU 19100. Identification of the short focused-system stand-off. Use the device instructions to confirm compatibility and handling.
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. Information related to various health, medical, and fitness conditions and their treatment is not meant to be a substitute for the advice provided by a physician or other medical professional.
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. [1]