Buy TENS Unit in Nigeria.

Which TENS-capable Chattanooga systems can I request in Nigeria?

Three current catalogue records are assigned to the TENS Unit category. Each link applies the Chattanooga brand, this category and a model-specific search query:

- Chattanooga Intelect Mobile 2 STIM, model 15-1202-INT
- Chattanooga Intelect Mobile 2 COMBO, model 15-1204-INT
- Chattanooga Intelect Transport 2 Combo, listed US SKU 4738

The product names are similar, so include the complete model or SKU in a request. Mobile 2 STIM is the stimulation-only configuration in this set. Mobile 2 COMBO combines stimulation and ultrasound. Transport 2 Combo also combines both modalities, but its listed 4738 code is the US-market listing; Chattanooga’s international page identifies a different 4778-INT reference. Franance should confirm which exact regional code and electrical configuration is proposed for the Nigerian destination before a buyer treats the offer as equivalent.

Browse the TENS Unit category for the current assignment set. Stock, price, market authorization, delivery, warranty and local service are not established by a category page; ask for destination-specific confirmation in the quotation.

What does TENS mean when buying physiotherapy equipment in Nigeria?

Transcutaneous electrical nerve stimulation is one electrical-stimulation mode identified by the manufacturer for these Chattanooga systems. The product record describes device functions and model identifiers. It does not establish which patients should receive treatment, how electrodes should be placed, what settings should be used, or what outcome a facility can expect. Those decisions belong to appropriately qualified clinicians following the exact instructions for use and facility protocols.

For procurement, translate the service requirement into a configuration question: does the department need a stimulation unit with TENS capability, a combined electrotherapy and ultrasound platform, or multiple separate devices? Identify whether staff need one or two stimulation channels, which documented waveforms matter to their service, and whether the ultrasound modality is in scope. Check these requirements against the manufacturer documentation for the exact item being quoted, not just a broad “TENS unit” label.

Do not use this guide to select a treatment protocol or to make a patient-specific decision. Before acceptance, ask the clinical lead to review the device’s indications, contraindications, warnings, intended users, electrode and lead compatibility, cleaning instructions and applicable service procedures. Ask for the current user manual for the actual regional model; feature descriptions for another variant do not replace its labeling.

Should I buy Intelect Mobile 2 STIM in Nigeria?

The Intelect Mobile 2 STIM is the stimulation-focused option among these three listings. Chattanooga identifies model 15-1202-INT as the STIM configuration and lists TENS and NMES waveforms. Its page describes a mobile unit that may be used with or without an optional cart; the cart can support an optional vacuum module. Chattanooga also lists optional accessories such as battery, leadwire kits and electrodes. Confirm the standard supply package and every optional item rather than assuming accessories shown in product material are included.

This model may fit a department that wants a dedicated electrotherapy configuration and does not require the product to provide ultrasound. That is a procurement distinction, not a clinical recommendation. Ask the clinical and biomedical engineering teams to verify the desired waveforms, number of channels, intended room or mobile workflow, current instructions, and maintenance and acceptance requirements.

The manufacturer product page lists a 100–240 V AC, 50/60 Hz input and dimensions and weight without the battery and cart. Confirm the actual nameplate, supplied power cord, battery configuration and accessory schedule for the offered regional model. View the exact 15-1202-INT listing and compare it with Chattanooga’s official STIM product page.

When should a facility compare Mobile 2 COMBO with STIM?

The Intelect Mobile 2 COMBO, model 15-1204-INT, combines electrotherapy with therapeutic ultrasound. Chattanooga lists two stimulation channels, five stimulation waveforms, and ultrasound frequencies of 1 MHz and 3 MHz. Its published overall dimensions and weight are stated without the battery and cart, both of which should be treated as configuration questions. Ask which applicator sizes are included and which are optional, and confirm whether a vacuum module or other accessories are part of the requested package.

Compare the COMBO with the STIM model only after the clinical service and biomedical team decide whether both modalities belong in the planned equipment scope. If ultrasound is not required, the additional modality may add an unnecessary configuration and accessory decision. If both are required, confirm the operating workflow, applicator size and included electrodes, leads, gel or consumables, cart, battery, room storage and servicing plan. The availability of two modalities does not by itself prove that the system meets a facility protocol.

Do not infer that “COMBO” means a particular application, treatment effectiveness or included accessory bundle. Review the current product instructions for the exact unit and ask Franance to make the offered package explicit. View the exact 15-1204-INT listing and compare with Chattanooga’s official Intelect Mobile 2 COMBO page.

What should I confirm about Intelect Transport 2 Combo?

The Intelect Transport 2 Combo is listed here under manufacturer US SKU 4738. Chattanooga’s US product page describes a two-channel electrotherapy and ultrasound combination system, with TENS among its listed electrical-stimulation waveforms and 1 MHz and 3.3 MHz ultrasound capability. The manufacturer also describes optional battery operation and cart. Its product page is useful for understanding the US-listed configuration, but it does not establish the market code, package or electrical supply Franance could quote to a Nigerian buyer.

Chattanooga’s international page uses SKU 4778-INT for a Transport 2 Combo. That difference makes exact identity especially important. Ask Franance to state the regional manufacturer code, input-power configuration, included leads and electrodes, ultrasound applicator, battery, cart and other accessories. Ask for the current user manual and regional declaration or conformity documents required by the facility. Do not assume that 4738 and 4778-INT are interchangeable just because both names include “Transport 2 Combo.”

If the request is for a TENS-capable system without ultrasound, compare against Mobile 2 STIM rather than selecting a combo model by name alone. View the exact SKU 4738 catalogue listing, Chattanooga’s US page for SKU 4738, and the international 4778-INT product page.

How is a TENS unit different from ultrasound therapy equipment?

TENS is an electrical-stimulation waveform or mode. Therapeutic ultrasound uses a separate applicator and modality. A device that combines them has multiple functions and a correspondingly broader accessory, training and maintenance scope. The Intelect Mobile 2 COMBO and Intelect Transport 2 Combo are both listed in the TENS category because their manufacturer pages include TENS-capable electrotherapy; the Transport 2 Combo also appears in the ultrasound therapy unit category. It is one product record with two category assignments, not two separate devices.

The STIM configuration is distinct in this product set because its listing specifies the electrical-stimulation unit and TENS/NMES waveforms without describing it as an ultrasound combination. If a department requires ultrasound, compare the combo configurations and exact applicator/package details. If it requires only electrotherapy, ask the clinical lead whether the STIM unit matches the written specification. Do not infer that a modality is present because another model in the Intelect family supports it.

Keep the procurement line items explicit: base unit, channels and waveforms documented for the exact model, leads, electrodes, ultrasound applicator and gel where applicable, battery, cart, power cord, software or data features, training and service. Ask the supplier to flag items that are optional, region-specific or excluded. This prevents category overlap from obscuring what the facility is actually requesting.

Which leads, electrodes and accessories should I specify?

List leads and electrodes separately from the device. Specify the number and type required by the service, connector compatibility, whether reusable or consumable electrodes are requested, replacement quantity and any requirements for compatible accessory documentation. Product photographs do not establish what is included in the quotation. Chattanooga describes different standard and optional accessories across its STIM and COMBO product pages, so use the exact model’s current accessory list.

For the two combo configurations, add ultrasound applicator requirements as separate line items. Ask for the exact applicator model and size, compatibility with the quoted system, and whether gel is included or needs to be sourced separately. For a portable or multi-room service, state whether the facility requires an optional battery, cart, storage, carry case or spare lead sets. Confirm how accessories are packed and whether any items need regular replacement.

Ask for a written package schedule that names manufacturer codes and quantities. If the department requires spare accessories, request separate pricing, availability and replacement lead time for each. Franance should confirm compatibility against the exact unit being quoted; do not mix lead sets, electrode types, applicators or consumables based only on visual similarity.

What site and power details matter for a Nigerian quote?

Give Franance the facility name, city and state, delivery access, quantities by location and requested delivery window. Identify whether each unit will remain on a treatment-room worktop, move between rooms or be used with a cart. Describe storage space, equipment trolley dimensions, room access and the process for securing and cleaning accessories. For a combo unit, consider where both the electrical-stimulation leads and ultrasound applicator will be stored between uses.

Ask the supplier to confirm the proposed unit’s voltage and frequency, supplied power cord and plug, battery option, charging arrangement, electrical safety documentation and any site conditions in the manufacturer instructions. Even when a manufacturer page lists a broad 100–240 V range, check the exact offered regional unit and nameplate. Do not assume a US SKU or plug configuration is appropriate for a Nigerian installation.

For multiple sites, request a location-by-location schedule of equipment, accessories, installation or handover scope, training request and service contact. Include any facility procurement documents or regulatory evidence that must accompany the quote. A catalogue listing does not confirm Nigerian stock, registration, delivery, warranty or local service coverage; obtain written destination-specific confirmation.

What should clinicians and biomedical teams review before procurement?

The clinical service should define the intended equipment role and review the current instructions for the exact configuration, including intended users, indications, contraindications, warnings, electrode placement limitations, interaction precautions, cleaning, storage and maintenance. This guide does not recommend a stimulation setting, duration, electrode location or use for any patient. Clinical decisions should remain with qualified professionals working within facility policy and the manufacturer’s instructions.

Biomedical engineering should verify the device identity, regional code, electrical supply, accessories, applied-part and safety documentation supplied for the actual unit, maintenance requirements and acceptance checks. For Mobile 2 COMBO or Transport 2 Combo, confirm the ultrasound applicator and its calibration or maintenance requirements from the relevant manual. For the STIM model, confirm all required leads and electrode accessories and their compatibility. Ask for the current revision of each applicable manual rather than relying on a product summary.

The FDA’s general information on electrical muscle stimulators notes the importance of clear device labeling and following device instructions, but it does not substitute for Nigerian requirements or Chattanooga’s model-specific documentation. Facilities should assess the exact proposed device under their own clinical, engineering and regulatory processes. Do not treat a manufacturer’s general feature page as a clinical protocol or proof of suitability for a specific patient group.

What belongs in a Franance TENS equipment quote request?

Use a model-specific request and separate required equipment from optional items. Include:

1. Exact model and code: Intelect Mobile 2 STIM 15-1202-INT, Intelect Mobile 2 COMBO 15-1204-INT, or Transport 2 Combo SKU 4738; for Transport 2, ask the supplier to confirm the regional code.
2. Whether the requirement is electrical stimulation only or a combination with therapeutic ultrasound.
3. Quantity, facility name, delivery city and state, access constraints and requested timing.
4. Required channels, manufacturer-listed waveforms or other documented configuration criteria for the service.
5. Leads, electrodes, ultrasound applicator and gel, compatible replacement accessories and quantities.
6. Battery, charger, power cord, cart, carry case, storage and mobility requirements.
7. Current user manual, regional model identification, conformity documents and any facility procurement records required.
8. Requested delivery, installation, handover, user training, maintenance, warranty and local support scope.

Ask the quotation to list included items, exclusions, optional equipment, exact manufacturer codes, destination-specific availability, price validity, delivery assumptions, warranty route, service contact and replacement-part process. Resolve any uncertainty about product code, power, accessory compatibility or regional configuration before accepting an order. Franance will follow up by phone or email and confirm the proposed commercial package in writing; submitting the request does not guarantee stock or supply.

Browse the exact STIM listing, Mobile 2 COMBO listing or Transport 2 Combo listing, then contact Franance for a TENS equipment quotation.

Can I buy Chattanooga TENS equipment online from Franance?

No. Franance receives quote orders for these medical devices and follows up by phone or email. Submit the product model, quantity, configuration, accessories and destination; the team will review the request and confirm availability and commercial terms in writing. There is no online payment or immediate purchase implied by a product listing.

Use the TENS Unit category to review the three assigned Chattanooga products. Compare the ultrasound therapy unit category separately if that is the main equipment need. Confirm the exact regional model and complete supply schedule before procurement approval. Clinical staff should separately review model-specific instructions and decide whether the equipment is appropriate for the service.