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Texua Physiotherapy & Wellness Equipment

Texua T301

Product Code: PAWE-EAPD-3222

An eight-inch touch screen, five probes, and half a bar to eight.

An eight-inch touch screen driving five shockwave probes, with energy from 0.5 to 8 bar in half-bar steps, frequency from 1 to 21 Hz, and a shot count set between 100 and 9,900. Just over thirteen kilograms on the bench.

Sections

Shockwave Therapy

Categories

Physiotherapy & Wellness Equipment

Condition

New

Origin

China

Seller Type

Certified Professional Seller

CE & ISO Certified

Global Shipping

Supplier: Medigear

Texua's T301 is a radial pressure wave device designed around an eight-inch touch screen and five probes. Energy runs from 0.5 to 8 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. The unit draws 350 W, measures 420 by 350 by 270 mm, weighs 13.25 kg and takes 220 V at 50 Hz or 110 V at 60 Hz. Pulse structure is not published: no waveform, rise time, pulse duration or energy equivalent appears, and nothing describes cooling or a duty cycle.

The screen changes the shape of a session rather than its physics. Each of the three parameters has a step size, and on a treatment titrated to what a patient will tolerate, those get adjusted repeatedly through the opening shots. Reading all three at once keeps the clinician looking at the treatment area with a hand free on the handpiece.

The sheet gives the screen size and nothing about what runs on it. No protocol library, no body map, no patient record, no session log, no export and no language options are mentioned. That matters beyond convenience. Shockwave therapy in the UK carries a standing expectation that outcomes are audited for every patient treated, and pressure, frequency and shot count are the three numbers that make a session reproducible in an audit entry. Whether this device retains them, or whether they go onto a form at the time, is the question to settle before the first list.

Medigear.uk lists the T301 for UK business buyers. Before ordering, ask what the screen actually displays and stores, the probe diameters and rated shot life, the device class with its declaration of conformity, and which voltage variant ships from the seller.

The T301 is best suited for conservative soft-tissue treatment, such as in physiotherapy departments, podiatry clinics, sports injury practices, and musculoskeletal services. Achilles tendinopathy, plantar fasciitis, tennis elbow and greater trochanteric pain syndrome are the indications shockwave therapy is most often used for, generally once conservative treatment has been tried and the problem has not resolved.

A screen earns its place in the rhythm of a session. Pressure comes up in half-bar steps during the opening shots while the clinician watches the patient rather than the machine, and the shot count runs down in view. Across a list of six or eight patients, each with different tolerance and a different probe, having all three in view is what keeps the session moving. The shot count runs down on screen as the treatment progresses.

Radial output shapes the clinical fit. Energy is highest at the skin and disperses with depth, which suits superficial tendon and muscle targets and behaves differently on deeper structures. A service planning deeper work should establish what this modality reaches before committing, because the specification makes no claim in either direction.

Buying runs through the usual routes. NHS musculoskeletal services, private physiotherapy and podiatry groups, sports medicine practices, and veterinary users each apply their own procurement rules, and a Class IIa or IIb device must clear clinical governance alongside finance. Conformity documentation is issued by the manufacturer and provided by the seller. Report adverse incidents involving the device to the MHRA through the Yellow Card scheme.

Three live parameters on one display

Pressure, frequency and shot count each carry a step size, and all three change during a session. An eight-inch display is large enough to hold them together without the operator hunting through levels, which matters when one hand is on the handpiece, and the other is on the patient.

Five probes settled at the point of order.

The probe count is published rather than left to the quotation, so the set arrives with the machine. On a device where probe face determines the treated area, having a range from day one lets a clinician match the head to the target without waiting on a separate order.

Increments fine enough to titrate

Half a bar and a single hertz are small enough steps to work up to what a patient will tolerate over the first hundred shots, which is how published protocols are written. The increment matters as much as the range on a treatment delivered by feel.

Ranges that encompass published protocols

Tendon work in the literature commonly runs 2.5 to 5 bar at 3 to 5 Hz for 1,500 to 3,000 shots. All three fall within the published ranges with headroom, so a service following a documented protocol can reproduce it without running the equipment to its limits.

A bench footprint one person can sit

At 420 by 350 by 270 mm and 13.25 kg, the unit fits a standard treatment room bench or trolley and moves between rooms without help. That suits services running shockwave in whichever room is free.

Dual rated voltage

Rated voltage covers 220 V at 50 Hz and 110 V at 60 Hz, which widens where a unit can be redeployed across a group, provided the variant supplied is confirmed when ordering.

Mains powered and nothing els.e

The device needs a socket. No gas, no water buffer, no plumbed supply and no consumable fluid reservoir, so room preparation comes down to a bench and a power point.

The open questions are all answerable in writing.ng

What the screen shows and stores, probe diameters and shot life, device class and certificate, registration, UK Responsible Person, voltage variant. Every one sits in the manufacturer's file already, and how completely the answers come back is itself information about the supplier.

Radial pressure wave modality

Pressure waves are generated pneumatically, with output quoted in bar. Energy is highest at the skin surface and disperses with depth. The specification uses neither the word radial nor the word focused.

Energy 0.5 to 8 bar

Output is adjustable across the full range in 0.5-bar increments, giving sixteen settings.

Frequency 1 to 21 Hz

Impact frequency is adjustable in single-hertz steps across the full range, giving twenty-one settings.

Shot count 100 to 9,900

The number of impacts per session is set in 100-impact increments, for 99 settings.

Eight-inch touch screen

Control is through an eight-inch touch screen. No resolution, interface description, protocol library, body map, language options or session record function is published.

Five shockwave probes supplied

Five probes are listed as included. No diameters, face profiles, intended applications or rated shot life are given for any of them.

350 W power draw

Input power is published at 350 W. No duty cycle, continuous-run limit or cooling arrangement is stated against it.

Unit dimensions 420 × 350 × 270 mm

The machine is published at those dimensions with a net mass of 13.25 kg.

Packed dimensions 545 × 455 × 425 mm

The packed size and mass are also published: 17 kg, with a shipping volume of roughly 0.105 cubic metres.

Dual rated voltage

Rated voltage is given as 220 V at 50 Hz or 110 V at 60 Hz. Whether a unit is switchable or built to one standard is not stated.

Pulse structure not published.

No waveform, rise time, pulse duration or energy equivalent in millijoules per square millimetre appears, so output cannot be mapped onto studies reporting energy flux density.

Cooling and duty cycle not published.d

Nothing describes cooling, a continuous-operation limit or a rest interval for a 350 W device delivering several thousand impacts in a session.

Handpiece and probe life not publish.ed

No rated shot life appears for the handpiece, the projectile or the probe faces, and no method of indicating wear is described.

Class, marking and registration not published.

No device class, no marking under UKCA or CE, no Approved Body number, no MHRA registration and no UK Responsible Person appears anywhere on the specification.

The T301 publishes its three output parameters with the step size attached to each, lists five probes as supplied, and puts an eight-inch touch screen on the front. The screen is the reason to look at it, and also the thing the specification says least about. Screen size is a dimension; what runs on it decides whether a clinician works from a protocol or from memory, and whether the session parameters end up on the device or on a form. Given that shockwave therapy carries a standing expectation of auditing outcomes for every patient treated, that is worth settling in writing. Medigear.uk lists the T301 for UK business buyers and can arrange delivery, installation, commissioning, familiarisation and service cover. Request what the screen displays and stores, the probe specifications and shot life, the device class with its declaration of conformity, and the voltage variant from the seller at quotation.

FAQ

Frequently Asked Questions

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

Unstated, and worth pinning down early. The specification gives an eight-inch touch screen and stops there. A screen of that size could carry a protocol library organised by indication, a body map, a live view of the three parameters, a session history, or simply three large numbers and a start button. Each of those is a different machine to work with. Ask for screenshots or a short video of the interface, the number of taps needed to change pressure mid-session, whether protocols can be saved and recalled, and what languages are available.

Nothing published says either way, and this is the question with consequences attached. Shockwave therapy in the UK comes with an expectation that clinical outcomes are audited for every patient treated, and an audit entry is only useful if it carries the parameters used. Pressure, frequency, shot count and probe are exactly those. If the device stores them, the audit becomes a matter of reading them off. If it does not, they go onto a clinic form during treatment, every time. Ask directly, and if the answer is that it stores them, ask whether they can be exported or only viewed.

Supplied, and otherwise undescribed. Publishing the count is more than this Class of specification usually offers, and it means the probe set is settled when the order is placed rather than afterwards. What is absent is what each probe is for. Face profile and diameter determine the treated area and how energy spreads from the contact point, so a set of five could span very different applications or offer variations on one. Ask for each probe by diameter and intended use, and whether further probes are available separately.

Not published, and on a ballistic device this governs the replacement cycle. The mechanism drives a projectile against a probe face thousands of times in a session, and both the projectile and the faces wear. A shot count running to 9,900 means a single long session uses a real share of a component's working life. Ask for the rated shot life of the handpiece and of each probe, how wear shows itself before it affects output, and what the replacement interval looks like expressed in sessions rather than months.

Radial, based on the evidence of the specification. Energy 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 outward from the skin. Focused devices are quoted in millijoules per square millimetre, concentrate their peak at a chosen depth, and use electromagnetic, electrohydraulic or piezoelectric generators. Radial energy is highest at the surface and disperses with depth. The sheet uses neither term, so confirm the modality and check it against the depth of the structures being treated.

They do, with headroom at the working end. Trial protocols for tendon indications commonly run between 2.5 and 5 bar, at 3 to 5 Hz, delivering 1,500 to 3,000 shots per session. All three sit inside the published ranges of 0.5 to 8 bar, 1 to 21 Hz and 100 to 9,900 shots. Half-bar and single-hertz increments are fine enough to work up to patient tolerance across the opening shots, which is how most protocols are written. Covering a protocol is not the same as being suitable for a given indication, which remains a clinical judgement.

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 Class IIb. Both classes require a UK Approved Body, so a numbered certificate exists or the device is not lawfully on the market. Registration with the MHRA is needed before it reaches the Great Britain market, and a manufacturer established outside the UK must appoint a UK Responsible Person whose details appear on the labelling or instructions. None of this is stated. Ask for all four.

The specification lists 220 V at 50 Hz or 110 V at 60 Hz and does not say which is supplied. A 110 V unit needs a transformer to run in a UK clinic, which raises its own electrical safety questions. Confirm the variant on the order along with the plug and lead, and ask whether the machine is switchable or built to one standard. Ask at the same time what electrical safety testing interval the manufacturer expects.

Nothing addresses it. A number on a screen is a setting rather than a measurement, and on a ballistic device the energy actually delivered falls as the projectile and probe faces wear. Without a verification routine, there is no way to know whether the same setting still produces the same output after a year of use. Ask what verification the manufacturer specifies, at what interval, who carries it out, and whether any output measurement can be taken on site.

Any service that needs the audit record held on the device and cannot get a straight answer on whether it is. Any clinic treating structures at depth, since radial output is weighted to the surface. Anyone unable to obtain the Class, certificate and registration, which are not optional at Class IIa or IIb. And any buyer who wants the probe specifications before committing, which is reasonable when five are supplied and none is described. For a physiotherapy or podiatry service treating surface tendon problems with an audit routine already running, the published ranges cover the protocols in the literature.