Buy Chattanooga Intelect Mobile 2 Ultrasound in Nigeria
To buy the Chattanooga Intelect Mobile 2 Ultrasound in Nigeria, request a written Franance quotation for the ultrasound-only set, model 15-1200-INT, and confirm the plug version, 5 cm² applicator, gel, any optional smaller applicator, battery or cart, and service documentation. Chattanooga lists 1 MHz and 3 MHz ultrasound, pulsed and continuous duty cycles, and a supplied 5 cm² applicator. It is intended for use under prescription and supervision by a licensed medical practitioner. The catalogue is quote-only; it does not take online payment or confirm price, stock, delivery timing or Nigerian service coverage.
Where can I request an Intelect Mobile 2 Ultrasound quote in Nigeria?
Review the Chattanooga Intelect Mobile 2 Ultrasound listing filtered to therapeutic ultrasound units and the ultrasound therapy unit category page. Send a Franance quotation enquiry for Chattanooga Intelect Mobile 2 Ultrasound. Include the facility name, destination state and city, quantity, intended physiotherapy setting, procurement contact and any clinical-engineering specification.
Franance follows up on enquiries by phone or email. Ask for a written quote naming the exact device and international set code, supplied applicator, gel and cord, plus any optional accessories as separately listed lines. Request delivery, orientation, warranty and service details that specifically apply to the Nigerian order. A product-page quote form does not mean local availability or a completed sale.
What is the ultrasound-only Intelect Mobile 2 configuration?
The Intelect Mobile 2 family has separate electro-stimulation-only, ultrasound-only and COMBO devices. This catalogue record is the ultrasound-only product, SKU 15-1200-INT. The manufacturer documentation distinguishes the ultrasound device head, model 15-0131, from international sets 15-1200 (EU plug) and 15-1201 (All Plug). Confirm the actual unit and cord in the offer. The suffix “INT” alone does not establish which regional plug or accessories will arrive.
The ultrasound version has no STIM output. Its brochure and product listing describe ultrasound therapy only; do not transfer TENS/NMES waveforms or STIM electrode contraindication details as if they were its primary function. The COMBO product is a separate model if both ultrasound and electrical stimulation are required. A cart, battery or extra applicator is optional unless the quotation explicitly includes it.
What ultrasound frequencies, duty cycles and applicator are listed?
Chattanooga lists dual frequencies of 1 MHz and 3 MHz, pulsed or continuous delivery, and pulsed duty cycles of 10%, 20%, 50% and 100% (continuous). The product page further describes pulse repetition rates and pulse duration, while the manufacturer specification table gives model-specific applicator output characteristics. Confirm the exact current datasheet and applicator type for the offered revision, especially where a written clinical-engineering requirement includes frequency, effective radiating area, output or duty-cycle settings.
The manufacturer lists a 5 cm² applicator as supplied with the ultrasound-only set. It lists 1 cm² and 2 cm² Mobile 2 applicators as optional accessories. Applicator sizes, effective radiating area and output details differ; a size label alone does not establish suitability for every required use. Ask the supplier to identify each applicator by part number and confirm that it is explicitly compatible with Intelect Mobile 2 Ultrasound. The manual warns that applicators from earlier Chattanooga ultrasound models do not work with the Mobile 2.
The device includes coupling feedback: Chattanooga says the user can monitor coupling audibly or by an LED and that the treatment-time indicator stops when the applicator uncouples. This is a feature description, not proof that technique, clinical dosage or treatment delivery will be correct in an individual session. Operators must follow the current manual and professional instruction.
What manufacturer-listed indications and contraindications must be reviewed?
The Chattanooga product page lists ultrasound indications including relief of pain associated with muscle spasm, joint contracture, ligament sprains, tendinitis and muscle sprain. These are the manufacturer’s listed indications, not recommendations for an individual patient, evidence that the unit will produce an outcome or a substitute for clinical assessment. Chattanooga states that the equipment should only be used under prescription and supervision by a licensed medical practitioner.
The current user manual includes mode-specific contraindications and precautions. Its listed contraindications include use over a cancerous lesion, an eye, a pregnant uterus, a healing fracture, or near bone growth centres before growth is complete; it also addresses known or suspected infection, particular cardiac and implanted-device circumstances, and MRI/CT environments. This is a concise procurement summary, not an exhaustive safety checklist. The exact language and context in the current regional instructions for use govern; clinical personnel must screen each case and use professional judgment.
The manual also lists precautions for certain conditions, tissue areas and applications, and calls for operation by a licensed healthcare professional who understands the warnings. Do not use the treatment presets or manufacturer indication list as a patient-specific treatment prescription. Franance sells equipment through quotation; this guide does not provide therapy instructions, diagnose or assess a condition, or claim regulatory approval in Nigeria.
Which applicator, gel and consumables should I specify?
The ultrasound-only set documentation lists a 5 cm² applicator, transmission gel, power cord, printed quick-start guide and USB drive. The Chattanooga product page also lists 1 cm² and 2 cm² Mobile 2 applicators and ultrasound gel as optional accessories. Confirm the exact quantities, bottle size, accessory references, and whether the standard applicator supplied is 1 MHz/3 MHz as required by the exact set. Do not assume a gel bottle shown in a product image is the same quantity or formulation included in a Nigerian quote.
For a clinic expecting regular use, ask about genuine compatible applicator replacement and gel replenishment, ordering references and cleaning instructions. The operator manual identifies alcohol-based cleaning for the applicator sound head and cautions to avoid the plastic section when disinfecting the aluminium surface. Follow the latest manufacturer instructions for the exact applicator and the facility’s infection-control protocol; do not apply unverified chemicals or procedures. Confirm inspection, cable integrity and maintenance checks before use according to the manual.
If the smaller heads are needed for a particular facility workflow, list each separately and request written compatibility confirmation. If the clinic expects a cart to hold applicators and gel, quote it as a separate accessory unless included. A COMBO set has a different included accessory schedule, so do not use its bill of materials as proof of what belongs in the ultrasound-only package.
What power, battery and room setup should I plan for in Nigeria?
The product page lists a 100–240 V AC input, 50/60 Hz and a maximum input current range. The manual instructs users to verify the actual voltage rating on the device plate before connection. Confirm the rated input, cord and outlet plug supplied for the Nigerian transaction, and have the facility’s biomedical or electrical team confirm outlet suitability and any power-conditioning need. Do not assume that “100–240 V” means any extension cord, plug adapter or unstable outlet is appropriate.
The optional Mobile 2 battery is not necessarily included. Ask whether it is offered for this version, its part number, availability with the quotation, charging instructions, storage requirements and operating limitations. If a cart is needed for moving between treatment rooms, confirm the Mobile 2 compatible cart and whether it is included. The small head-unit footprint does not establish the table, room, cart or patient-space requirements of a particular clinic.
Plan a stable work surface, enough clearance for the operator and patient, safe cable routing, accessible power isolation and storage for gel and applicators. For outreach use, request the manufacturer’s guidance on carrying, environmental conditions and transport protection. The device is not a fixed installation; however, a mobile design does not remove the need for safe placement, cleaning and supervision.
How do applicator size and coupling feedback affect the quote?
The manufacturer’s applicator options include 1 cm², 2 cm² and 5 cm² heads. Ask the clinical team to specify which applicator sizes and frequencies the facility intends to procure; the supplier should then confirm the compatible parts, included head, and any separate order reference. The manufacturer describes effective radiating area and maximum output values by head and frequency, so avoid comparing two applicator sizes based only on the nominal area printed in the name.
Chattanooga describes audible and LED coupling feedback and a treatment-time indicator that stops when the applicator is uncoupled. Ask for the operator demonstration to include indicator behavior, treatment review and end-of-session steps. The facility’s clinical lead should decide whether these interface features fit local workflow. They do not replace correct preparation, coupling medium, operator contact and movement, patient screening or clinical supervision.
If a replacement head is being purchased, provide the existing device model and serial number and request compatibility confirmation for the exact head. Previous-generation Chattanooga ultrasound applicators are not compatible according to the Mobile 2 manual. Do not assume that a generic 1/3 MHz applicator or another Chattanooga-branded head can be substituted.
What records, software and data functions should I verify?
The product page describes treatment data storage, Bluetooth import/export capability, custom protocols, a suggested protocol setup interface and anatomical resources. These features can vary with software version and the user should confirm details in the current IFU. If the clinic needs to retain treatment records or transfer protocols, ask which Windows application and operating-system versions are supported, what data are exported, how Bluetooth is paired, and how the facility will protect the data under its own privacy rules.
Do not interpret Bluetooth import/export as direct EMR or hospital information system compatibility. No named Nigerian hospital system or network integration is established by the product listing. Ask for a demonstration or written compatibility statement if data transfer is essential; involve the facility IT and privacy teams before relying on a workflow. If the clinic will use the instrument without data transfer, document its own record-keeping process separately.
At handover, record the model and serial number, software version, manual revision, applicator part numbers, power rating, battery or cart if supplied, and any service documentation. Ask the vendor to identify what training is included and how software updates and current IFUs are obtained. The product’s suggested settings are not a substitute for a clinician’s prescription or judgment.
What installation, training and maintenance support should the quote state?
Ask whether the quotation includes inspection on arrival, setup, function checks, user orientation, biomedical-engineering handover or a demonstration. State who delivers it, its format, location and scope. The manufacturer’s online education and demo references do not mean an onsite visit, course or local service is bundled with a Nigerian order.
Request the current operator manual, quick-start guide, applicator cleaning instructions, battery instructions where relevant, troubleshooting steps and service contact. The manual specifies cleaning and inspection steps for the applicator and system; the facility should use those instructions and its infection-prevention policy. Ask for any recommended periodic checks or calibration requirements for the exact configuration. Do not assume a particular interval, local calibration provider or field-service technician unless the written quote confirms it.
Have the quote state warranty period, territory, exclusions, repair process, spare-part availability and transportation responsibilities for the particular Nigerian sale. The manufacturer’s public product page does not promise Nigerian coverage. Ask who to contact for faults, how the device is protected while awaiting repair and whether replacement equipment is available under any service arrangement. Keep the user and biomedical team’s acceptance records with the asset documentation.
How should I compare the Ultrasound model with STIM and COMBO?
Choose the catalogue record that matches the facility’s modality specification. Intelect Mobile 2 Ultrasound is the ultrasound-only model; Intelect Mobile 2 STIM provides electrical stimulation; COMBO is the separate model for both. The manufacturer's instructions and accessories differ. This guide does not recommend a treatment modality for a patient or facility; a licensed clinical lead should define that need.
Compare the exact model and set code, frequencies, duty cycles, compatible applicator sizes, supplied head, gel, display and data functions, battery or cart, power cord, cleaning procedures, training and service. Check the package line by line. If a quote offers an ultrasound accessory separately, ensure it is a Mobile 2 compatible part and not from an older generation. If both modalities are needed, price and evaluate the dedicated COMBO version separately; do not assume an ultrasound-only head can be upgraded into a COMBO without manufacturer confirmation.
The Chattanooga ultrasound therapy unit listing filtered to 15-1200 identifies the exact catalogue record. The ultrasound therapy unit category page contains other equipment, which may use different applicators, frequencies and operating procedures. Compare actual manuals, not category labels alone.
What should I include in a Nigerian Intelect Mobile 2 Ultrasound quote request?
Send the facility and delivery details, state and city, quantity, department, contact person and desired delivery window. Specify 15-1200-INT, EU or all-plug set requirement if known, included 5 cm² head, additional 1 cm² or 2 cm² applicators, gel quantities, battery, cart, software/data requirements, user orientation and warranty/service needs. Add any engineering or power specification and tell the supplier whether the unit will be used across rooms or in outreach settings.
Ask Franance for a written itemized quotation identifying the unit head and set code, plug and cord, applicators and gel, accessories, current manuals, delivery, user training, warranty and service terms. Request a statement of what is included and excluded, and ask for written compatibility confirmation for any replacement or optional applicator. Do not assume inventory, lead time, local regulatory approval or support availability.
Open the exact Chattanooga brand/category/model filtered listing, then send the Franance quotation enquiry. Franance follows up by phone or email; the listing does not support online payment.
What is verified about this model and what remains open?
Chattanooga’s official Intelect Mobile 2 Ultrasound product page identifies SKU 15-1200-INT, its ultrasound-only configuration, 1 MHz and 3 MHz frequencies, duty-cycle options, supplied 5 cm² applicator, optional smaller heads, main power input and listed product features. The manufacturer lists 15-0140, 15-0141 and 15-0142 for the 1 cm², 2 cm² and 5 cm² Mobile 2 applicators, respectively, and cautions that previous-generation applicators are incompatible. Its current Intelect Mobile 2 IFU, linked in the product Documents section provides the safety, clinical-use and maintenance instructions for the family. Obtain the current regional manual and follow its exact contraindications before use.
The Franance record assigns this model to the ultrasound therapy unit category. It does not state the serial number, supplied regional plug, final package contents, extra applicators, battery, cart, software version, warranty territory, delivery or support. Confirm those in the written Nigerian quote. Nothing here is a treatment protocol or patient-specific advice.