Scan the product code
A user, distributor, nurse, biomedical technician, or support agent scans a QR code on the device, package, or support page and opens the support assistant built for that product.
Field Support Memory Pilot
For products such as infusion pumps, in vitro diagnostic analyzers, monitors, respiratory equipment, or service-heavy devices, the same setup, alarm, accessory, maintenance, and troubleshooting questions often repeat. This package converts approved sources into support answers, troubleshooting cards, escalation rules, and Product ID support memory.
This is a co-built pilot, not an off-the-shelf chatbot. We build it around one company's device, customers, support team, field service workflow, approved source material, and escalation rules.
What the user experiences
The first version can be shown as a web demo before it becomes a production support tool. The goal is to prove the support workflow and review boundary with one real customer product family.
A user, distributor, nurse, biomedical technician, or support agent scans a QR code on the device, package, or support page and opens the support assistant built for that product.
They can type, speak, or upload a photo. The infusion pump alarm example is only a sample scenario; each pilot uses the customer's own product, users, support process, and source set.
The assistant uses approved manuals, training material, support notes, and troubleshooting cards. If the source does not support an answer, it routes the question instead of guessing.
If the issue is not resolved, technical support receives the symptom, selected steps, images, likely category, urgency, and field-service preparation notes.
Example scenario
In this sample, a user reports an infusion pump alarm after changing tubing. The same pattern could apply to another medical device product. The assistant does not make a repair determination. It asks the approved checks, records what happened, and packages the unresolved issue for the right support owner.
The session closes with the checked source, the steps taken, the answer used, and any follow-up note the manufacturer wants to preserve.
The support team sees likely issue category, selected checks, user-provided images, model context, and possible parts or tools to prepare.
The case routes to technical support, clinical support, complaint intake, field service, RA/QA, or legal / regulatory review based on the escalation matrix.
Repeated questions become support intelligence: training gaps, unclear instructions, service-procedure review points, or Product ID memory updates.
Pilot deliverables
The pilot is built from approved or customer-reviewed material. It is designed with the customer, not handed over as a generic tool. Unsupported, off-label, clinical, complaint, regulatory, or high-risk questions route to the right owner.
Records and memory
With the manufacturer's configuration and consent model, the support flow can preserve the session facts that matter for customer service, technical support, field service, complaint intake, and Product ID review.
Pricing hypothesis
The USD 4,800 pilot is the first build together: one company's product, one support boundary, one reviewed source set, and one working flow the team can test with real support scenarios.
USD 1,500-2,500
One narrow support scenario, one source set, and a small demo flow for prospect validation or internal review.
USD 4,800-8,000
A co-built pilot for one company product or product family: controlled answer library, troubleshooting cards, escalation map, QR support flow, and support intelligence report.
USD 1,500-3,500 / month
New source intake, answer updates, repeated-question review, escalation-rule updates, and Product ID support memory writeback.
60-second demo video script
This storyboard is ready for a quick screen recording or generated explainer after the page is reviewed.
A user has a repeated support issue and does not want to search a manual or wait on hold for a basic approved check.
They scan the code, say what happened, and upload a photo of the screen or connection area.
The assistant only uses approved support sources. It walks through the checked steps and stops when the question moves outside the source boundary.
If the issue is not solved, support receives the symptom, selected checks, photos, likely issue category, and field-service preparation notes.
The company sees which questions repeat, what training is missing, and which issues may need service, complaint, or RA/QA review.
TrueMedDevice organizes approved sources, support answers, escalation rules, issue records, and Product ID memory proposals. The manufacturer's support, field service, quality, regulatory, clinical, and legal reviewers approve final support content and decide complaint, repair, regulatory, quality, clinical, and legal actions.
The assistant must not determine device safety, effectiveness, compliance, complaint status, Medical Device Reporting (MDR) status, corrective and preventive action (CAPA) need, recall need, repair conclusion, clinical action, or use outside approved instructions.