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Texua Physiotherapy & Wellness Equipment

Texua 2201

Product Code: PAWE-EAPD-3440

With a 10.4-inch screen, the patient can see seven probes.

A radial pressure wave device with a 10.4-inch touchscreen and seven probes, energy from 0.5 to 10 bar in half-bar steps, frequency from 1 to 21 Hz, and a shot count of 100 to 9,900 per session.

Sections

Shockwave Therapy

Categories

Physiotherapy & Wellness Equipment

Condition

New

Origin

China

Seller Type

Certified Professional Seller

Size:

430 × 350 × 350 mm

CE & ISO Certified

Global Shipping

Supplier: Medigear

Built by Texua, the 2201 is a radial pressure wave device aimed at services that explain the treatment before delivering it. Energy runs from 0.5 to 10 bar in half-bar increments, frequency from 1 to 21 Hz in single-hertz steps, and the shot count from 100 to 9,900 in hundreds. Seven probes are listed as supplied. The console draws 380 W, carries a 10.4-inch touch screen, measures 430 by 350 by 350 mm and weighs 20.7 kg. No waveform, rise time, pulse duration or energy equivalent is published, and nothing describes cooling or a duty cycle.

The screen is the entry worth reading closely. The product photograph shows an anatomical figure displayed on it, and a panel that size, turned toward the couch, lets a clinician show a patient where the probe will go and what the settings mean for shockwave; that is more than a courtesy. NICE attaches special arrangements for consent to this procedure across tendon indications, and asks that patients understand the uncertainty about its efficacy before agreeing.

The guidance goes further in places. For greater trochanteric pain syndrome, patients should be told about the possibility of pain during and after treatment and the risk that symptoms may worsen. A screen helps that conversation happen properly. It does not replace what the guidance actually asks for: clear written information, with NICE's own public information recommended alongside.

Medigear.uk lists the 2201 for UK business buyers. Before ordering, request what the screen runs, the probe specifications and rated shot life, the device class with its declaration of conformity, and an inventory of the carton from the seller.

The 2201 fits services where explaining shockwave is part of delivering it. Hospital musculoskeletal and orthopaedic outpatient departments, sports medicine clinics, podiatry services, and physiotherapy departments treating Achilles tendinopathy, patellar and other knee tendinopathies, plantar fasciitis, tennis elbow, and greater trochanteric pain syndrome all work under the same NICE expectation: special arrangements for governance, consent, and audit.

The consent part of that is where the screen earns its place. A patient who can see an anatomical figure with the treatment site marked, and the pressure and shot count that will be used, has a better grasp of what they are agreeing to than one who has been told in passing. For greater trochanteric pain, where NICE specifically wants patients warned about pain during and after treatment and the risk of symptoms worsening, a structured explanation at the couch is exactly what the guidance intends.

None of that replaces the written element. NICE asks for clear written information, and recommends its own public information for the purpose. The screen supports the conversation, and the leaflet completes it, so a service introducing the 2201 should have both ready before the first list.

Radial output shapes the clinical fit. Energy is highest at the skin and diminishes with depth, suiting superficial insertions at the heel, knee and elbow. Procurement runs through trust services, private practices and sports medicine providers under their own rules, with a Class IIa or IIb device clearing clinical governance alongside finance. Adverse incidents go to the MHRA through the Yellow Card scheme.

A 10.4-inch touch screen

Large enough to turn towards the couch and be read from where the patient is lying. For a procedure where NICE expects the patient to understand the uncertainty before agreeing, a display the patient can actually see is a practical aid, not a feature for its own sake.

An anatomical figure on screen

The product photograph shows a body map on the display. Pointing at the treatment site on a figure is clearer than describing it, particularly for the lateral hip and the Achilles insertion, where patients often have no clear picture of what is being treated.

Seven probes supplied

The count is published, so the set arrives with the console. The probe face governs the treated area, and seven gives a clinician options for a narrow tendon insertion and a broader region such as the greater trochanter.

Full 0.5 to 10 bar in half-bar steps

Twenty energy settings, fine enough to titrate to tolerance across the opening shots and wide enough to reproduce published protocols with room either side.

Parameters that can be shown and recorded

Stepped energy, frequency, and shot count make each session reproducible, and on a large screen those three numbers are visible to both parties. That supports the audit NICE asks for as well as the conversation that precedes it.

Ranges that encompass published protocols

Tendon protocols in the literature commonly run 2.5 to 5 bar at 3 to 5 Hz for 1,500 to 3,000 shots. All three fall within the published ranges.

Stable once sited

At 20.7 k,g the console stays where it is placed and does not shift under its own vibration or when a lead is caught. For a service treating in one room, that is one less thing to manage.

The open questions are all answerable in writing.ng

What the screen runs, the probe specifications and shot life, the carton contents, the class and certificate, the registration and the voltage variant. are already in the manufacturer's factory.

Radial pressure wave modality

Compressed air drives the handpiece, and the output is stated in bar. Peak energy sits at the point of contact and tapers off as the wave travels inward.

Energy: 0.5 to 10 bar

Twenty positions across the range, each half a bar apart.

Frequency 1 to 21 Hz

Twenty-one positions, one hertz apart, from the slowest rate to the fastest.

Shot count 100 to 9,900

The session length in impacts is chosen in hundreds, which gives ninety-nine possible counts.

10.4-inch touch screen

Control is through a 10.4-inch touch screen. The product photograph shows an anatomical figure, but no interface, preset, record, rd or language function is described.

Seven probes supplied

Listed as included. No diameters, face profiles, intended applications or rated shot life are given.

380 W power draw

The mains draw is 380 W. How long it may run continuously, and how it sheds heat, are both left unsaid.

Console dimensions 430 × 350 × 350 mm

A near-cube of about fifty-three litres, weighing 20.7 kg without its packaging.

Packed dimensions 545 × 455 × 425 mm

Around 0.105 cubic metres and 43 kg once boxed, which means whatever travels alongside the console outweighs it.

Dual rated voltage

Either 220 V at 50 Hz or 110 V at 60 Hz, with no indication of whether one build handles both.

Pulse structure not published.

The shape of each impact goes undescribed: no waveform, no rise time, no duration and no figure in millijoules per square millimetre.

Cooling and duty cycle not published.d

Whether the console needs resting between patients, and for how long, is not addressed.

Handpiece and probe life not published. The number of times the handpiece cable or any probe face will take before replacement is never stated, and nothing warns of wear.

Class, marking and registration not published.

The sheet is silent on the class, on any UKCA or CE mark, on an Approved Body, on MHRA registration and on who acts as UK Responsible Person.

The screen is the reason to look at this console, and it's not cosmetic. Shockwave carries a standing NICE expectation that patients understand the uncertainty about efficacy before they agree, and for greater trochanteric pain, that they are warned about pain during and after treatment and the risk of symptoms worsening. A 10.4-inch display with an anatomical figure turned towards the couch makes that conversation clearer. It doesn't replace the clear written information the guidance asks for, and the sheet doesn't say what the screen actually runs. The carton, at 43 kg, needs a handling plan before it arrives. Medigear.uk lists the 2201 for UK business buyers and can arrange delivery, installation, commissioning, familiarisation and service cover. Request the interface description, probe specifications, and device class from the seller in the quotation.

FAQ

Frequently Asked Questions

Everything buyers need to know about sourcing medical equipment through MediGear.

More than a signature. Across tendon indications, NICE says the procedure should be used only with special arrangements for clinical governance, consent, and audit or research. Clinicians should inform the governance leads in their organisation, ensure that patients understand the uncertainty about efficacy, provide clear written information, and audit outcomes for everyone treated. NICE's own public information is recommended for that written element. The explanation belongs before agreement, not afterwards.

No, and it is worth being clear about that. A 10.4-inch display turned toward the patient makes the explanation easier to give and follow, and an anatomical figure on screen lets a clinician point to the site rather than describe it. The guidance asks for clear written information the patient can take away and read. Use the screen to guide the conversation; hand over the leaflet to meet the requirement.

Specifically, the possibility of pain during and after treatment, and the risk that symptoms may get worse. NICE spells that out for this indication in addition to the general uncertainty about efficacy. Radial shockwave delivers its peak at the skin surface over the lateral hip, and the treatment can be uncomfortable. A patient who has been told that in advance is better placed to decide, and to tolerate the session if they go ahead.

Unstated, beyond what the photograph shows. The product image shows an anatomical figure on the display, suggesting a body map or site selector. Whether it offers protocol presets by indication, a record of each session, adjustable text size, language options or a patient-facing view is not described. Ask for screenshots or a short video of the interface, and ask whether a session can be logged against the site treated.

Forty-three kilograms packed against 20.7 kg net leaves over twenty-two kilograms that is not the console, which is more than the console itself. Seven probes, a handpiece, leads and any case or stand may account for some of it. Ask what the carton contains, whether a trolley or stand is included, and whether the load can be split into lighter packages. The answer also decides how it gets from the loading bay to the room.

Not the carton, and the console only with care. UK law sets no maximum lifting weight; the Manual Handling Operations Regulations require employers to avoid hazardous handling where reasonably practicable and assess what remains. HSE's guideline figures of 25 kg for men and 16 kg for women are filters for when that assessment is needed, applying close to the body between knuckle and shoulder height and falling to around 10 and 7 kg at floor level. The carton exceeds both outright, and the console exceeds the women's figure in ideal conditions.

Radial, going by the specification. Output quoted in bar and a pneumatically driven handpiece place it in the radial pressure-wave class, where a projectile strikes a probe face, and the wave spreads from the skin surface. Focused devices are specified in millijoules per square millimetre and concentrate energy at a chosen depth. Radial energy is greatest at the surface and falls with depth, which suits superficial tendon insertions and sits less comfortably with deeper structures.

Listed as supplied and otherwise undescribed. Probe face and diameter decide the treated area and how energy spreads from the contact point, so the set matters more than the count. For Achilles and patellar tendon work, the relevant question is which probe suits a narrow insertion; for the lateral hip, which suits a broader area. Ask for each probe by diameter and intended application, and for the rated shot life of each.

Under UK MDR 2002, an active therapeutic device intended to administer energy falls under Rule 9, giving Class IIa unless the energy may be administered in a potentially hazardous way, in which case it is Class IIb. Both need a UK Approved Body and a numbered certificate, MHRA registration before the device reaches the Great Britain market, and a UK Responsible Person where the manufacturer is outside the UK. None of that appears on the sheet. Ask for all four.

Any service without the governance, consent and audit arrangements that NICE expects for shockwave, since a screen does not supply them. Anyone treating deep structures, because radial output is weighted to the surface. Any team that cannot plan a two-person or trolley delivery for a 43 kg carton. And any buyer who needs the probe specifications before committing. For a hospital or outpatient service that already explains shockwave properly and wants the screen to help, the configuration fits.