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Texua Physiotherapy & Wellness Equipment

Texua T202

Product Code: PAWE-EAPD-3216

Five probes supplied, half a bar to eight, and no screen.

Five shockwave probes supplied with the machine, 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. Twelve kilograms, 350 watts, no screen.

Sections

Shockwave Therapy

Categories

Physiotherapy & Wellness Equipment

Condition

New

Origin

China

Seller Type

Certified Professional Seller

CE & ISO Certified

Global Shipping

Supplier: Medigear

The T202 is Texua's radial pressure wave device for services working across more than one treatment room. 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. Five shockwave probes are listed as supplied. The unit draws 350 W, measures 420 by 350 by 270 mm, weighs 12 kg, and takes 220 V at 50 Hz or 110 V at 60 Hz. Pulse structure is absent: no waveform, rise time, pulse duration or energy equivalent appears, and nothing describes cooling or a duty cycle.

One line on the specification does more work than the rest. Screen size reads "no screen", stated as plainly as any dimension. That is worth respecting as an honest declaration, and it decides two things. It decides how a clinician sets three parameters, each with a defined step size, because something has to indicate where those settings sit, and the sheet describes no indicator at all. It also decides where the session record lives.

That second point carries weight in the UK. Shockwave therapy comes with 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. With nothing on the machine holding them, they have to be written down at the time, every time, by whoever is treating. That is workable, and it needs to be built into the clinic's paperwork before the first list, not after.

Medigear.uk lists the T202 for UK business buyers. Before ordering, request the probe diameters and rated shot life, how the three settings are indicated without a screen, the device class with its declaration of conformity, and which voltage variant ships from the seller.

The T202 suits services that treat soft tissue in any available room. Physiotherapy departments, podiatry clinics, sports injury practices and musculoskeletal services all run lists across several rooms, and a twelve-kilogram machine moves with the clinician instead of the clinician moving patients to it. Shockwave therapy is most often used for Achilles tendinopathy, plantar fasciitis, tennis elbow, and greater trochanteric pain syndrome, generally after conservative treatment has been tried without resolving the problem.

Five probes widen what one machine covers within that list. Probe face and diameter determine the treated area and how energy spreads from the contact point. So, a set supplied with the machine can handle trigger-point work on a muscle belly and a focal tendon insertion in the same visit, without ordering anything first. What each probe suits is a question for the seller, since the sheet gives a count and no descriptions.

Radial output shapes where it fits clinically. 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 clears 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.

Five probes settled at the point of order.

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

Three parameters, each with its step size published

Pressure moves in half-bar increments, frequency in single hertz, shot count in hundreds. On a treatment titrated to what a patient will tolerate, the increment matters as much as the range, because it sets how finely a clinician can work up during the opening shots of a session.

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 with headroom, so a service following a documented protocol can reproduce it without pushing the equipment to its limits.

Twelve kilograms and a carry handle

The machine weighs 12 k,g and the product photograph shows a handle on the top face. A unit one person can pick up and carry is a unit that goes to the patient, which suits a list spread across several rooms or a service running clinics on more than one site.

Little packaging to dispose of

Net mass is 12 kg against a packed 16 kg, so four kilograms is case and protection. Goods-in handles one carton of roughly 0.109 cubic metres, and there is not much to break down afterwards.

Mains-powered and nothing else.

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

Dual rated voltage

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

The open questions are all answerable in writing.

Probe diameters and shot life, how the settings are indicated, device class and certificate, registration, UK Responsible Person, voltage variant. Every one sits in the manufacturer's file already. How complete the answers are 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 sheet uses neither the word radial nor 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, giving 99 settings.

Five shockwave probes supplied

The machine includes five probes. No diameters, face profiles, intended applications or rated shot life are given for any of them.

No screen

Screen size is published as none. The specification describes no alternative indicator for the three settable parameters, and no on-device record of a completed session.

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 12 kg. The product photograph shows a carry handle, which the written specification does not mention.

Packed dimensions 545 × 475 × 420 mm

The packed size and packed mass of 16 kg are both published, giving a shipping volume of roughly 0.109 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 published.

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.d

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 sheet.

The T202 publishes its three output parameters with the step size attached to each, lists five probes as supplied, and states plainly that there is no screen. That last line is the honest one and the consequential one. It means the settings need some other indicator, which the sheet does not describe, and it means the session record lives on paper or in the clinic's own system rather than on the machine. Given that shockwave therapy carries a standing expectation of auditing outcomes for every patient treated, that record has to be designed rather than assumed. Medigear.uk lists the T202 for UK business buyers and can arrange delivery, installation, commissioning, familiarisation and service cover. Request the probe specifications and shot life, how the settings are indicated, the device class with its declaration of conformity, and the voltage variant from the seller in the quotation.

FAQ

Frequently Asked Questions

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

This is the first question to ask the seller, and the sheet does not answer it. Three parameters are published with defined step sizes: pressure in half-bar increments, frequency in single hertz, and shot count in hundreds. Numbers with step sizes imply something that displays or indexes them, whether that is a segment display, a row of indicators, a detented dial or a printed scale. The specification says only that there is no screen, and describes no alternative. Ask what the operator actually looks at when setting each of the three, and whether the shot count decrements visibly as a session runs.

Onto paper or into the clinic's own system, because nothing on the machine is described as holding it, that matters more here than it would on a general piece of equipment. Shockwave therapy in the UK carries an expectation that clinical outcomes are audited for every patient treated, and an audit entry needs the parameters used. Pressure, frequency and shot count are precisely those parameters. Build a session form that captures all three, along with the probe used, and make recording it part of the treatment routine rather than something done afterwards from memory.

Supplied, and otherwise unspecified. The count is published, which is more than this class of sheet usually offers, and it means the transmitter set is settled at the point of order rather than becoming a second conversation. What is missing is what each one is. Probe diameter and face profile determine the treated area and how energy spreads from the contact point, so a set of five could cover very different jobs or five variations on one. Ask for each probe by diameter and intended application, and whether further probes are available.

Not published, and on a ballistic device this is the figure that governs the replacement cycle. The mechanism fires a projectile against a transmitter face thousands of times per session, and both the projectile and the faces wear. A shot count running to 9,900 means a single long session can consume a meaningful share of a component's working life. Ask for the rated shot life of the handpiece and of each probe, how wear shows itself, and what the replacement interval looks like expressed in sessions.

Radial, judging by the specification. Energy quoted in bar and a pneumatically driven handpiece place it in the radial pressure-wave class, where a projectile strikes a transmitter, and the wave spreads outward from the skin. Focused devices are quoted in millijoules per square millimetre, concentrate peak energy at a chosen depth, and use electromagnetic, electrohydraulic or piezoelectric generators. Radial energy is highest at the surface and disperses as it travels. The sheet uses neither word, so confirm the modality and check it against the depth of the structures being treated.

They do, with room to spare at the working end. Trial protocols for tendon indications commonly sit between 2.5 and 5 bar, at 3 to 5 Hz, delivering 1,500 to 3,000 shots in a session. All three fall 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 over the first hundred 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, which assigns Class IIa unless the energy may be administered in a potentially hazardous way, in which case it is Class IIb. Both classes need a UK Approved Body, so a numbered certificate exists or the device is not lawfully on the market. Registration with the MHRA is required 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 sheet 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 setting is not a measurement, and on a ballistic device the energy actually delivered falls as the projectile and transmitter faces wear. Without a verification routine, there is no way to know whether the same setting is still producing 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 treatment record held on the device, since nothing here describes that. Any clinic treating structures at depth, because 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 to insist on given five are supplied, and none are described. For a physiotherapy or podiatry service treating surface tendon and muscle problems with its own paper record already running, the published ranges cover the protocols in the literature.