Insurance & Coding Notes for Clinicians: Documenting Medical Necessity Early

Every clinician knows that good care begins with good documentation. Yet, when it comes to prosthetic or rehabilitation patients, what you write in the first few days after surgery can shape the entire course of their recovery — not only medically but financially.

A prosthesis, no matter how advanced, is useless if the insurance paperwork fails to justify why it’s needed. For many patients, especially in India’s evolving healthcare system, reimbursement or funding decisions depend entirely on how early and how clearly the physician’s notes establish medical necessity.

This article is designed for clinicians who want to bridge the gap between good medicine and smart documentation. It explains how to structure your notes, use the right codes, and phrase medical necessity statements in ways that insurance reviewers understand — without turning your charting into a bureaucratic chore.

The goal is simple: help patients receive the care they deserve, faster, with fewer denials and delays.

The Role of Documentation in Medical Necessity

Why Documentation Decides Access

Insurance companies do not see patients.

Insurance companies do not see patients. They see paperwork. The only way they can understand a person’s medical reality is through the physician’s words. That means your notes are more than records — they’re a translation of need into language that payers can accept.

A single missing line in an early note — for example, not mentioning “loss of limb function affecting activities of daily living” — can delay or deny prosthetic coverage for weeks.

Good documentation doesn’t mean writing more. It means writing smarter — focusing on functional impact, not just diagnosis.

Defining Medical Necessity

In simple terms, medical necessity is proof that a treatment, device, or procedure is essential for the patient’s health, function, or quality of life — not a convenience or luxury.

In prosthetic care, that means showing:

  • Why the patient needs a prosthesis (functionally and medically).
  • Why other options (like assistive aids or conservative therapy) are not sufficient.
  • How the device will improve or restore function.

Your narrative should make that logic visible. Every line you write is a bridge between medicine and policy.

The Clinician’s Responsibility

Doctors sometimes assume that the prosthetist or billing team will handle insurance language. But payers give the greatest weight to physician documentation. A prosthetist can describe the device, but only the doctor can establish necessity for it.

This makes the first few entries after surgery crucial. Each progress note, wound update, or rehab referral should gently build the case for why the prosthesis is not optional but medically required.

Writing the Story Behind the Device

Focus on Function, Not Just Anatomy

Many early notes focus on surgical success — “amputation completed without complication,” “stump healing well,” “pain controlled.” While essential, these phrases don’t tell insurers why a prosthesis is needed.

Instead, connect anatomy to ability. For example:

  • “Patient unable to perform daily self-care tasks such as dressing or eating due to loss of hand function.”
  • “Residual limb length allows good potential for prosthetic fitting to restore independent ambulation.”

These lines shift your documentation from observation to justification.

Describing the Impact on Daily Life

Insurance reviewers need a vivid picture of limitation. Avoid abstract terms like “functional loss.” Instead, describe how the amputation affects specific actions.

Examples include:

  • Difficulty maintaining balance or transferring.
  • Dependence on caregivers for toileting or dressing.
  • Inability to return to previous employment or vocational tasks.

A good note reads like a short story — one that makes the reader understand what the patient cannot do without the prosthesis and what they could do with it.

The Early Narrative

From the first postoperative note, plant the seed of necessity.

  • “Rehabilitation potential: excellent. Prosthetic fitting anticipated upon wound healing.”
  • “Patient motivated and showing good muscle control suitable for early prosthetic training.”

These brief observations establish that a prosthesis is part of the medical plan, not an afterthought. Later, when documentation is reviewed for authorization, these statements prove the continuity of intent.

Aligning With Insurance Requirements Early

Understanding the Language of Payers

Every insurance provider, whether government or private, works with definitions and checklists. They’re looking for specific words: medical necessity, functional limitation, physician recommendation, rehabilitation plan.

Doctors don’t have to memorize policy documents, but understanding the tone helps. Payers appreciate concise, objective statements supported by measurable data.

For example, rather than “patient is doing well and can start therapy soon,” write, “patient able to perform 5-minute unsupported sitting; upper limb strength sufficient for initial prosthetic assessment.”

This converts general impressions into quantifiable progress — a language insurers can process.

The Timeline of Documentation

Most insurance evaluations occur in stages. Early surgical notes set the foundation, mid-rehab notes confirm progress, and discharge summaries close the loop. Each stage should reaffirm medical necessity in a new way.

  • Post-op notes should highlight potential for prosthetic rehabilitation.
  • Rehab progress notes should demonstrate improvement due to preparatory therapy.
  • Final reports should confirm readiness and ongoing benefit expectation.

When every phase points in the same direction, the file tells a coherent story — and coherent stories rarely get denied.

Including Objective Measurements

Where possible, use numbers: wound dimensions, range of motion, muscle strength grades, or ambulation distance.

For example:
“Residual limb edema reduced by 60% over 2 weeks with compression. Range of motion at knee 0–110°. Patient able to perform sit-to-stand with standby assistance.”

Each metric supports the case that healing is progressing toward prosthetic readiness.

Early Coordination With the Prosthetist

Building a Shared Documentation Chain

Insurance reviewers prefer cohesive records

Insurance reviewers prefer cohesive records — surgeon, physician, and prosthetist all speaking the same language.

When you coordinate early, the prosthetist can mirror your phrasing. If your notes say “Patient demonstrates upper limb control suitable for myoelectric training,” the prosthetist can reference that same statement when requesting device approval.

Consistency signals legitimacy. Discrepancies trigger review.

Physician Sign-Off on Prosthetic Plan

Whenever possible, include a formal medical recommendation in your note before the prosthetist files their authorization request. A simple line like, “Prosthetic fitting indicated for restoration of independent ambulation,” acts as a physician endorsement.

Without it, some payers reject claims citing lack of doctor direction.

Documenting Communication

Briefly record collaboration in your chart:
“Discussed prosthetic plan with certified prosthetist. Initial fitting scheduled upon full epithelialization.”

This not only proves coordination but also reinforces that the decision was clinically guided.

Writing for Reviewers, Not Just Records

Avoiding Medical Jargon

Many insurance officers are not doctors. They are trained in claims review, not clinical terminology. Keep language simple, direct, and specific.

Instead of “post-operative myodesis with viable musculature suitable for early prosthetic adaptation,” write, “muscles healing well and strong enough to support prosthetic fitting soon.”

Simple phrasing doesn’t reduce credibility; it increases clarity.

Framing Progress as Purpose

Each note should connect progress to outcome. Healing, strength, and motivation should all point toward one direction — independence through prosthetic use.

Example:
“Patient reports reduced phantom pain and improved limb tolerance. Continuing therapy to prepare for prosthesis application within 3–4 weeks.”

This sentence tells reviewers that improvement has a goal — fitting — and that it’s being pursued under supervision.

Using Positive Prognosis Statements

Insurance reviewers need confidence that the device will work. If your note reflects optimism grounded in medical observation, approvals come faster.

“Given stable wound and preserved joint mobility, prognosis for successful prosthetic use is good.”

That one line does more for approval than a full paragraph of technical data.

Documenting Barriers Without Losing Momentum

Being Honest, But Hopeful

Every patient faces barriers — infection, comorbidities, emotional distress. It’s important to note them, but equally important to record the plan to overcome them.

For example:
“Wound shows mild delayed healing due to diabetes. Glycemic control improved; expect readiness for prosthetic evaluation in two weeks.”

By documenting action along with problem, you keep the narrative moving forward.

Addressing Psychosocial Readiness

Insurance reviewers often look for evidence that the patient can benefit emotionally and mentally from prosthetic rehabilitation. Include small, simple observations:
“Patient demonstrates motivation, attends all sessions, and expresses desire to regain work function.”

Such lines show not just physical but psychological suitability — a strong justification for necessity.

Documenting Family Involvement

If caregivers are trained or supportive, note it. Insurance providers see family participation as a positive predictor for successful prosthesis use.

Example:
“Patient’s spouse trained in stump hygiene and compression wrapping. Family demonstrates good understanding of rehabilitation plan.”

It signals stability and commitment — key factors in approving device funding.

Coding Fundamentals for Prosthetic Documentation

Why Codes Matter Early

Coding isn’t just for billing teams. The moment you assign an accurate diagnostic or procedure code, you begin building the reimbursement structure for the prosthesis.

When coding is delayed or incomplete, the prosthetic claim often lacks an anchor. Early, correct codes allow the entire chain — physician, prosthetist, therapist — to work under the same reference.

Choosing Accurate Diagnostic Codes

For limb loss cases, documentation should always include both the primary condition and its cause. For example:

  • “Traumatic amputation, right below elbow, due to crush injury.”
  • “Amputation secondary to diabetic gangrene, left below knee.”

This dual clarity links medical history with necessity. Insurers see not just the event but the underlying reason for device support.

Linking Procedure and Diagnosis Codes

Whenever wound revision, grafting, or debridement is performed, pair the procedure code with the corresponding diagnosis code.

For instance, if a revision surgery occurs, record:
“Procedure: Residual limb revision due to delayed healing (T87.81).”

This shows that each intervention supports the path toward eventual prosthetic readiness, not an isolated episode.

Coding for Complications or Delays

Accurate secondary coding — for infection, edema, or contracture — demonstrates ongoing clinical supervision. It reassures insurers that challenges are managed, not ignored.

But balance is key: too many uncontextualized complication codes may imply poor progress. Add narrative context whenever possible:
“Minor infection (T87.43) treated with oral antibiotics; wound now stable.”

It signals control, not chaos.

Structuring Physician Notes for Medical Necessity

Building a Clear Template

Most clinicians write progress notes in a routine pattern

Most clinicians write progress notes in a routine pattern, but small changes in wording can turn a standard update into an insurance-ready record. A good template follows a simple, logical flow — patient context, medical findings, functional limitations, plan, and expected outcome.

For example:

Subjective: Patient reports difficulty performing personal hygiene and self-care due to loss of right hand. Motivated for rehabilitation.

Objective: Residual limb healing well with no drainage. Range of motion preserved. Grip and pinch potential in remaining limb adequate.

Assessment: Functional deficit limits independence in daily activities. Early prosthetic training indicated to restore self-care capability.

Plan: Continue wound observation for one week. Refer to prosthetist for assessment once epithelialization complete. Anticipated readiness within 10–14 days.

This format meets both clinical and insurance standards without adding extra work. It tells a story of necessity in four short sections.

Writing with the Future in Mind

When documenting early, think of the future authorization request as the reader. Every line you write today will support or weaken that application. A sentence like “patient to be reviewed for prosthetic suitability post healing” establishes an early intent that payers appreciate.

Later, when the prosthetist submits for approval, that line will act as your prior medical justification. It shows that prosthetic care was always part of the treatment plan, not a late addition.

Keeping the Tone Objective

Insurance reviewers prefer facts over adjectives. Instead of writing “patient doing very well,” use measurable indicators: “wound 95% closed, no signs of infection, full range of motion at knee.”

This tone feels less emotional but more credible. A factual narrative strengthens every authorization.

Recording Progress That Supports Coverage

Tracking Rehabilitation Milestones

Physicians and physiatrists should document each major improvement, even if small. Notes like “patient tolerated standing for 10 minutes with balance support” or “muscle strength improved from grade 3/5 to 4/5” show measurable progress.

Such records prove that therapy is working and that a prosthesis will further enhance function. When you later declare that a prosthetic device is required, the insurer already sees the upward curve.

Connecting Each Step to the Prosthetic Goal

Every therapy, wound care measure, or compression activity can be linked subtly to the ultimate goal. Example: “Continued stump wrapping to prepare for optimal socket fit.”

This phrasing shows that even basic interventions are part of a continuum leading to prosthetic success. It demonstrates intention, not random treatment.

Reinforcing Motivation and Compliance

Include simple observations about patient engagement: “attends all sessions,” “practices exercises daily,” “expresses strong interest in walking again.”

These details convince payers that the patient will benefit from the device, not abandon it. They also protect you from future audits questioning the value of the prosthesis.

Avoiding Common Documentation Errors

Missing Functional Justification

A frequent cause of denial is documentation that focuses only on medical condition, not on the resulting disability. Writing “below-knee amputation due to diabetes” is accurate but incomplete. Add one more line: “Unable to ambulate independently; prosthesis required to regain mobility and prevent further deconditioning.”

That single sentence converts a diagnosis into a necessity.

Copying Old Notes

Repeated or identical entries across visits suggest poor monitoring. Insurers view this as lack of active management. Instead, vary each note to reflect fresh observation — even a small update such as “swelling decreased” or “pain improved.”

This shows continuous supervision and validates ongoing medical involvement.

Skipping Multidisciplinary Mentions

When physical therapy, occupational therapy, or prosthetic assessments are involved, record them. Even a brief note like “coordinated with PT for strength training prior to fitting” signals teamwork.

For insurers, collaboration equals quality of care. It shows that prosthetic use is part of an integrated rehabilitation plan, not a one-time decision.

Real-World Example: The Power of Early Documentation

Consider two similar patients with lower-limb amputations. Both had uncomplicated healing, similar age, and same surgical level.

The first patient’s notes simply read: “Amputation healing well, follow-up in one week.”

The second patient’s notes included: “Wound healing without infection. Ambulation potential excellent. Plan for early prosthetic assessment once volume stable. Goal: independent walking.”

When insurance approval was sought, the first file triggered multiple queries and required extra letters. The second was approved in one submission.

The difference lay in foresight — one doctor recorded a wound, the other recorded a journey.

Preparing for Preauthorization and Audit

The Value of Early Data Capture

From the first visit, start collecting measurable

From the first visit, start collecting measurable evidence that proves improvement — photographs, circumference logs, physiotherapy scores. Label them in the patient file.

If an insurance company audits later, this documentation will support your clinical reasoning. Reviewers prefer seeing progress supported by images and numbers, not just words.

Maintaining Consistency Across Reports

Ensure your discharge summary matches the story told in previous notes. If early notes mention “excellent rehabilitation potential,” the final report should not say “limited progress due to poor motivation.”

Inconsistencies invite questions. Consistency reflects control and clarity.

Preparing a Summary for the Prosthetist

Before the prosthetist submits documentation, provide them with a short physician summary highlighting the medical indications. A paragraph like this suffices:

“Patient with right below-knee amputation following infection. Residual limb well healed. Muscle control and joint mobility preserved. Motivated for independent ambulation. Prosthetic fitting recommended to restore functional mobility and prevent deconditioning.”

This shared language ensures that both the doctor and the prosthetist speak with one clinical voice.

Physician–Insurer Communication

Responding to Queries

When insurers request clarification, respond promptly and precisely. Avoid long replies; one clear, factual sentence works best.

Example: “Yes, patient is medically stable and suitable for early prosthetic fitting as per rehabilitation assessment dated 10 March.”

Speed and clarity show professionalism and prevent rejections due to lack of response.

Avoiding Over-Explanation

Adding too much technical detail can confuse nonmedical reviewers. Stick to essentials: the condition, its effect on function, and the expected benefit of treatment.

A simple note such as “prosthesis medically required to restore safe walking” often communicates better than a dense paragraph of jargon.

Building Long-Term Relationships

Insurers remember clinicians who provide clean, complete documentation. Over time, approvals become faster. Building rapport through reliable paperwork is as important as medical expertise.

Every correct code and concise explanation adds to your reputation for trustworthy submissions.

Educating the Medical Team

Creating Awareness Among Juniors and Residents

In teaching hospitals, residents often write the first drafts of medical notes. Train them early in documenting medical necessity, not just clinical facts. Show them how a single line can affect reimbursement outcomes.

Example exercise: compare two sample notes and explain why one would pass insurance review and the other would not. This builds awareness that clarity is part of care.

Collaboration With Nursing Staff

Nurses record daily observations — pain scores, wound checks, activity levels. Encourage them to note small functional improvements that can support future justification: “Patient sat independently for 10 minutes.”

These entries may seem minor but strengthen your overall medical narrative.

Including Physiotherapists in the Documentation Flow

Therapy notes often contain rich functional data. Coordinate with your physiotherapy team so their documentation mirrors your medical direction. If you state “goal: prepare for early prosthetic fitting,” their notes should reinforce that trajectory.

A synchronized file carries far more weight than separate voices.

Building Patient Understanding

Explaining the Role of Documentation

Patients rarely realize that their progress notes affect their insurance claims. Doctors can educate them in simple terms:

“The more we document your improvements and needs, the easier it becomes to get your prosthesis approved. Your participation in therapy and follow-ups helps us show that you’re ready.”

When patients understand this link, they cooperate better during assessments and attend reviews more reliably.

Encouraging Transparency

Invite patients to share any difficulties with wound care, pain, or finances early. Recording these concerns honestly shows insurers that you are managing the case comprehensively.

“Patient expressed financial concern regarding prosthetic cost. Discussed insurance application in progress.”

This line demonstrates empathy and accountability.

Reinforcing Their Role in Justification

Explain that compliance itself proves necessity. “Your regular exercises and attendance show that the prosthesis will truly benefit you.” Patients who know this often take ownership of their own record.

Robobionics’ Perspective: Turning Paperwork Into Progress

The Reality of Modern Prosthetic Care

At Robobionics, we work with clinicians across India

At Robobionics, we work with clinicians across India who face the same challenge — how to balance patient care with the growing demand for insurance documentation. We’ve seen incredible doctors lose weeks of time because of unclear notes and equally seen simple, structured documentation open doors for faster approvals.

Our message is simple: medical necessity is not paperwork; it’s a clinical truth written clearly.

Supporting Clinicians With Ready Templates

We provide hospitals and rehabilitation centers with sample documentation formats that fit real Indian insurance frameworks. These templates guide doctors on phrasing, coding, and linking therapy progress with device eligibility.

Each form is designed to be quick to fill, but powerful in proving need. When clinicians use consistent templates, both patients and payers benefit.

Partnership With Physicians

Our prosthetists and care coordinators often assist doctors in collecting early evidence — wound photographs, functional scores, and therapy milestones. Together, we build a timeline that insurers can easily review.

By keeping all stakeholders aligned, the process becomes less about defending claims and more about demonstrating care.

The Bigger Picture

Clear documentation means faster fittings, fewer denials, and better patient outcomes. It means doctors spend less time chasing approvals and more time healing.

For patients, it transforms the waiting period into progress. They move from anxiety to activity sooner.

For us at Robobionics, this is not just administrative improvement; it’s ethical care — ensuring no patient loses their chance at independence because of missing words on a page.

Closing Thoughts

The physician’s pen is the first prosthesis. It bridges patients to their devices through the language of necessity.

When doctors write with clarity, insurers read with trust. When care and compliance move together from day one, prosthetic fitting becomes faster, smoother, and fairer.

Good documentation is not bureaucracy; it’s compassion written down. Every detail you record is a step closer to mobility, dignity, and independence for the person waiting on the other end of the process.

At Robobionics, we stand beside every clinician who turns documentation into advocacy. Together, we can make early prosthetic access not a privilege but a right — delivered through precision, partnership, and purpose.

Leave a Comment

Your email address will not be published. Required fields are marked *

Partner With Us

REFUNDS AND CANCELLATIONS

Last updated: November 10, 2022

Thank you for shopping at Robo Bionics.

If, for any reason, You are not completely satisfied with a purchase We invite You to review our policy on refunds and returns.

The following terms are applicable for any products that You purchased with Us.

Interpretation And Definitions

Interpretation

The words of which the initial letter is capitalized have meanings defined under the following conditions. The following definitions shall have the same meaning regardless of whether they appear in singular or in plural.

Definitions

For the purposes of this Return and Refund Policy:

  • Company (referred to as either “the Company”, “Robo Bionics”, “We”, “Us” or “Our” in this Agreement) refers to Bionic Hope Private Limited, Pearl Haven, 1st Floor Kumbharwada, Manickpur Near St. Michael’s Church Vasai Road West, Palghar Maharashtra 401202.

  • Goods refer to the items offered for sale on the Website.

  • Orders mean a request by You to purchase Goods from Us.

  • Service refers to the Services Provided like Online Demo and Live Demo.

  • Website refers to Robo Bionics, accessible from https://www.robobionics.in

  • You means the individual accessing or using the Service, or the company, or other legal entity on behalf of which such individual is accessing or using the Service, as applicable.

Your Order Cancellation Rights

You are entitled to cancel Your Service Bookings within 7 days without giving any reason for doing so, before completion of Delivery.

The deadline for cancelling a Service Booking is 7 days from the date on which You received the Confirmation of Service.

In order to exercise Your right of cancellation, You must inform Us of your decision by means of a clear statement. You can inform us of your decision by:

  • By email: contact@robobionics.in

We will reimburse You no later than 7 days from the day on which We receive your request for cancellation, if above criteria is met. We will use the same means of payment as You used for the Service Booking, and You will not incur any fees for such reimbursement.

Please note in case you miss a Service Booking or Re-schedule the same we shall only entertain the request once.

Conditions For Returns

In order for the Goods to be eligible for a return, please make sure that:

  • The Goods were purchased in the last 14 days
  • The Goods are in the original packaging

The following Goods cannot be returned:

  • The supply of Goods made to Your specifications or clearly personalized.
  • The supply of Goods which according to their nature are not suitable to be returned, deteriorate rapidly or where the date of expiry is over.
  • The supply of Goods which are not suitable for return due to health protection or hygiene reasons and were unsealed after delivery.
  • The supply of Goods which are, after delivery, according to their nature, inseparably mixed with other items.

We reserve the right to refuse returns of any merchandise that does not meet the above return conditions in our sole discretion.

Only regular priced Goods may be refunded by 50%. Unfortunately, Goods on sale cannot be refunded. This exclusion may not apply to You if it is not permitted by applicable law.

Returning Goods

You are responsible for the cost and risk of returning the Goods to Us. You should send the Goods at the following:

  • the Prosthetic Limb Fitting Centre that they purchased the product from
  • email us at contact@robobionics.in with all the information and we shall provide you a mailing address in 3 days.

We cannot be held responsible for Goods damaged or lost in return shipment. Therefore, We recommend an insured and trackable courier service. We are unable to issue a refund without actual receipt of the Goods or proof of received return delivery.

Contact Us

If you have any questions about our Returns and Refunds Policy, please contact us:

  • By email: contact@robobionics.in

TERMS & CONDITIONS

Last Updated on: 1st Jan 2021

These Terms and Conditions (“Terms”) govern Your access to and use of the website, platforms, applications, products and services (ively, the “Services”) offered by Robo Bionics® (a registered trademark of Bionic Hope Private Limited, also used as a trade name), a company incorporated under the Companies Act, 2013, having its Corporate office at Pearl Heaven Bungalow, 1st Floor, Manickpur, Kumbharwada, Vasai Road (West), Palghar – 401202, Maharashtra, India (“Company”, “We”, “Us” or “Our”). By accessing or using the Services, You (each a “User”) agree to be bound by these Terms and all applicable laws and regulations. If You do not agree with any part of these Terms, You must immediately discontinue use of the Services.

1. DEFINITIONS

1.1 “Individual Consumer” means a natural person aged eighteen (18) years or above who registers to use Our products or Services following evaluation and prescription by a Rehabilitation Council of India (“RCI”)–registered Prosthetist.

1.2 “Entity Consumer” means a corporate organisation, nonprofit entity, CSR sponsor or other registered organisation that sponsors one or more Individual Consumers to use Our products or Services.

1.3 “Clinic” means an RCI-registered Prosthetics and Orthotics centre or Prosthetist that purchases products and Services from Us for fitment to Individual Consumers.

1.4 “Platform” means RehabConnect, Our online marketplace by which Individual or Entity Consumers connect with Clinics in their chosen locations.

1.5 “Products” means Grippy® Bionic Hand, Grippy® Mech, BrawnBand, WeightBand, consumables, accessories and related hardware.

1.6 “Apps” means Our clinician-facing and end-user software applications supporting Product use and data collection.

1.7 “Impact Dashboard™” means the analytics interface provided to CSR, NGO, corporate and hospital sponsors.

1.8 “Services” includes all Products, Apps, the Platform and the Impact Dashboard.

2. USER CATEGORIES AND ELIGIBILITY

2.1 Individual Consumers must be at least eighteen (18) years old and undergo evaluation and prescription by an RCI-registered Prosthetist prior to purchase or use of any Products or Services.

2.2 Entity Consumers must be duly registered under the laws of India and may sponsor one or more Individual Consumers.

2.3 Clinics must maintain valid RCI registration and comply with all applicable clinical and professional standards.

3. INTERMEDIARY LIABILITY

3.1 Robo Bionics acts solely as an intermediary connecting Users with Clinics via the Platform. We do not endorse or guarantee the quality, legality or outcomes of services rendered by any Clinic. Each Clinic is solely responsible for its professional services and compliance with applicable laws and regulations.

4. LICENSE AND INTELLECTUAL PROPERTY

4.1 All content, trademarks, logos, designs and software on Our website, Apps and Platform are the exclusive property of Bionic Hope Private Limited or its licensors.

4.2 Subject to these Terms, We grant You a limited, non-exclusive, non-transferable, revocable license to use the Services for personal, non-commercial purposes.

4.3 You may not reproduce, modify, distribute, decompile, reverse engineer or create derivative works of any portion of the Services without Our prior written consent.

5. WARRANTIES AND LIMITATIONS

5.1 Limited Warranty. We warrant that Products will be free from workmanship defects under normal use as follows:
 (a) Grippy™ Bionic Hand, BrawnBand® and WeightBand®: one (1) year from date of purchase, covering manufacturing defects only.
 (b) Chargers and batteries: six (6) months from date of purchase.
 (c) Grippy Mech™: three (3) months from date of purchase.
 (d) Consumables (e.g., gloves, carry bags): no warranty.

5.2 Custom Sockets. Sockets fabricated by Clinics are covered only by the Clinic’s optional warranty and subject to physiological changes (e.g., stump volume, muscle sensitivity).

5.3 Exclusions. Warranty does not apply to damage caused by misuse, user negligence, unauthorised repairs, Acts of God, or failure to follow the Instruction Manual.

5.4 Claims. To claim warranty, You must register the Product online, provide proof of purchase, and follow the procedures set out in the Warranty Card.

5.5 Disclaimer. To the maximum extent permitted by law, all other warranties, express or implied, including merchantability and fitness for a particular purpose, are disclaimed.

6. DATA PROTECTION AND PRIVACY

6.1 We collect personal contact details, physiological evaluation data, body measurements, sensor calibration values, device usage statistics and warranty information (“User Data”).

6.2 User Data is stored on secure servers of our third-party service providers and transmitted via encrypted APIs.

6.3 By using the Services, You consent to collection, storage, processing and transfer of User Data within Our internal ecosystem and to third-party service providers for analytics, R&D and support.

6.4 We implement reasonable security measures and comply with the Information Technology Act, 2000, and Information Technology (Reasonable Security Practices and Procedures and Sensitive Personal Data or Information) Rules, 2011.

6.5 A separate Privacy Policy sets out detailed information on data processing, user rights, grievance redressal and cross-border transfers, which forms part of these Terms.

7. GRIEVANCE REDRESSAL

7.1 Pursuant to the Information Technology Rules, 2021, We have given the Charge of Grievance Officer to our QC Head:
 - Address: Grievance Officer
 - Email: support@robobionics.in
 - Phone: +91-8668372127

7.2 All support tickets and grievances must be submitted exclusively via the Robo Bionics Customer Support portal at https://robobionics.freshdesk.com/.

7.3 We will acknowledge receipt of your ticket within twenty-four (24) working hours and endeavour to resolve or provide a substantive response within seventy-two (72) working hours, excluding weekends and public holidays.

8. PAYMENT, PRICING AND REFUND POLICY

8.1 Pricing. Product and Service pricing is as per quotations or purchase orders agreed in writing.

8.2 Payment. We offer (a) 100% advance payment with possible incentives or (b) stage-wise payment plans without incentives.

8.3 Refunds. No refunds, except pro-rata adjustment where an Individual Consumer is medically unfit to proceed or elects to withdraw mid-stage, in which case unused stage fees apply.

9. USAGE REQUIREMENTS AND INDEMNITY

9.1 Users must follow instructions provided by RCI-registered professionals and the User Manual.

9.2 Users and Entity Consumers shall indemnify and hold Us harmless from all liabilities, claims, damages and expenses arising from misuse of the Products, failure to follow professional guidance, or violation of these Terms.

10. LIABILITY

10.1 To the extent permitted by law, Our total liability for any claim arising out of or in connection with these Terms or the Services shall not exceed the aggregate amount paid by You to Us in the twelve (12) months preceding the claim.

10.2 We shall not be liable for any indirect, incidental, consequential or punitive damages, including loss of profit, data or goodwill.

11. MEDICAL DEVICE COMPLIANCE

11.1 Our Products are classified as “Rehabilitation Aids,” not medical devices for diagnostic purposes.

11.2 Manufactured under ISO 13485:2016 quality management and tested for electrical safety under IEC 60601-1 and IEC 60601-1-2.

11.3 Products shall only be used under prescription and supervision of RCI-registered Prosthetists, Physiotherapists or Occupational Therapists.

12. THIRD-PARTY CONTENT

We do not host third-party content or hardware. Any third-party services integrated with Our Apps are subject to their own terms and privacy policies.

13. INTELLECTUAL PROPERTY

13.1 All intellectual property rights in the Services and User Data remain with Us or our licensors.

13.2 Users grant Us a perpetual, irrevocable, royalty-free licence to use anonymised usage data for analytics, product improvement and marketing.

14. MODIFICATIONS TO TERMS

14.1 We may amend these Terms at any time. Material changes shall be notified to registered Users at least thirty (30) days prior to the effective date, via email and website notice.

14.2 Continued use of the Services after the effective date constitutes acceptance of the revised Terms.

15. FORCE MAJEURE

Neither party shall be liable for delay or failure to perform any obligation under these Terms due to causes beyond its reasonable control, including Acts of God, pandemics, strikes, war, terrorism or government regulations.

16. DISPUTE RESOLUTION AND GOVERNING LAW

16.1 All disputes shall be referred to and finally resolved by arbitration under the Arbitration and Conciliation Act, 1996.

16.2 A sole arbitrator shall be appointed by Bionic Hope Private Limited or, failing agreement within thirty (30) days, by the Mumbai Centre for International Arbitration.

16.3 Seat of arbitration: Mumbai, India.

16.4 Governing law: Laws of India.

16.5 Courts at Mumbai have exclusive jurisdiction over any proceedings to enforce an arbitral award.

17. GENERAL PROVISIONS

17.1 Severability. If any provision is held invalid or unenforceable, the remainder shall remain in full force.

17.2 Waiver. No waiver of any breach shall constitute a waiver of any subsequent breach of the same or any other provision.

17.3 Assignment. You may not assign your rights or obligations without Our prior written consent.

By accessing or using the Products and/or Services of Bionic Hope Private Limited, You acknowledge that You have read, understood and agree to be bound by these Terms and Conditions.