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Texua Physiotherapy & Wellness Equipment

Texua T606+2

Product Code: PAWE-EAPD-3523

Pressure in half-bar steps, shots in hundreds — every session dosed on one screen.

Repeat courses for heel, elbow, and shoulder pain use the same dose each visit. This pneumatic unit sets a pressure of 0.5–10 bar, a pulse rate of 1–21 Hz and a preset shot count on one 8-inch touchscreen.

Sections

Shockwave Therapy

Categories

Physiotherapy & Wellness Equipment

Condition

New

Origin

China

Seller Type

Certified Professional Seller

Size:

360 × 410 × 305 mm

CE & ISO Certified

Global Shipping

Supplier: Medigear

Texua's T606+2 is a radial shockwave therapy unit designed around step-by-step dose control. Its energy scale is rated in bar, the unit for a pneumatically driven applicator, and runs from 0.5 to 10 bar in 0.5-bar steps. Pulse frequency runs from 1 to 21 Hz in 1 Hz steps, and a preset shot count runs from 100 to 9,900 in steps of 100. Settings are made on an 8-inch touchscreen, seven probes are listed, rated power is 380 W, and the unit is offered for 220 V 50 Hz or 110 V 60 Hz supplies. The datasheet publishes no energy flux density, no standard configuration list and no handpiece service life.

Twenty pressure settings, twenty-one pulse rates and a shot count fixed before the applicator touches the skin mean a clinician can write a session down and repeat it exactly at the next visit. That matters because NICE asks for audit and careful consent where shockwave therapy is used for plantar fasciitis and Achilles tendinopathy, and a recorded dose is the starting point for both. The limit is plain: bar describes the driving pressure inside the applicator, not the energy reaching the tissue, so a protocol quoted in mJ/mm² cannot be transferred to this unit without per-probe data from the manufacturer.

The cabinet weighs 18.5 kg and carries the touchscreen. Product photography shows two handpieces holstered on the right-hand side. The published specification describes one shockwave probe set, and the "+2" suffix in the model name is not explained anywhere on the sheet.

The unit measures 360 × 410 × 305 mm, in the axis order published. Medigear.uk can arrange delivery, commissioning and service cover. Request the handpiece service interval and kit price, per-probe energy data, the full packing list and the declaration of conformity from the seller before ordering.

The T606+2 belongs in musculoskeletal physiotherapy departments, sports medicine clinics, podiatry services and orthopaedic outpatient settings, wherever chronic tendon and fascia problems are treated in courses of several sessions. The conditions most often treated with radial shockwave are plantar fasciopathy, lateral elbow tendinopathy, Achilles tendinopathy, greater trochanteric pain syndrome and calcific tendinopathy of the shoulder.

The evidence deserves an honest reading. NICE found no major safety concerns with shockwave therapy for refractory plantar fasciitis and Achilles tendinopathy, but judged the efficacy evidence inconsistent and recommended special arrangements for clinical governance, consent, and audit or research. Its 2022 guidance on calcific shoulder tendinopathy, now republished as HealthTech guidance 645, goes further and recommends use only in research. Individual trials point both ways. A confirmatory multicentre trial of 245 patients with chronic plantar fasciitis reported significantly better pain, function and quality of life after three sessions of radial shockwave than after placebo. A double-blind Norwegian trial published in 2024 found that radial shockwave, sham shockwave and a standardised exercise programme, each added to advice and customised foot orthoses, produced no significant difference in activity pain at six months.

For a buyer, that points to a specific use: refractory cases that have already had a fair trial of exercise and load management, treated within a written protocol and audited outcome measures. The unit's shot counter and stepped pressure support exactly that kind of record-keeping. It suits pathways where patient selection is careful and the clinical team is prepared to measure results.

The conformity documentation those procurement routes require comes from the manufacturer and is provided by the seller.

Dose is set in small, repeatable steps.

Pressure moves in 0.5 bar increments, pulse rate in 1 Hz increments,s and the shot count in blocks of 100. A clinician can therefore write a session down as three numbers and deliver the same session at the next visit, which is the basis of any audited treatment course.

A shot count fixed before treatment starts.

The preset count, adjustable from 100 to 9,900, defines the session length before the applicator touches the skin. This supports the consent and audit arrangements NICE requires, because the planned dose and the delivered dose can be recorded against the same figure.

Every parameter on one screen

Pressure, frequency and shot count are set on a single 8-inch touchscreen. Staff rotating through a clinic learn one interface, and the next patient's settings are visible at a glance before treatment begins.

Seven probes to match the treatment area

The unit lists seven probes. Once the seller confirms their diameters and intended uses, the set lets a clinician match the probe to the structure being treated and the patient's tolerance.

Headroom at the top of the pressure scale

The scale reaches 10 bar. The radial trial arm summarised in NICE's shoulder overview ran at 1.5 to 3.0 bar, so the upper range is available to be used with judgement, and more pressure is not automatically a better treatment. The value lies in having the whole range available when a protocol calls for it.

Two main variants for sites worldwide

The unit is offered for 220 V 50 Hz and 110 V 60 Hz supplies. Clinics on either mains standard can specify the version they need at order, avoiding the cost and risk of running a medical device through a voltage converter.

A cabinet one person can reposition

At 18.5 kg and 360 × 410 × 305 mm, the unit sits on a bench or trolley top, and one staff member can move it between treatment rooms. Delivery of the 43 kg carton still needs two people.

Running costs that can be pinned down before purchase

Applicator wear dominates the lifetime cost of any pneumatic shockwave unit. Asking for the rated shot life, service kit price and spares lead time at quotation turns an open-ended expense into a figure that fits the business case.

Pneumatic pressure generator

The energy scale is rated in bar, identifying a pneumatically driven ballistic applicator. The datasheet does not describe the air source, so confirm the compressor arrangement with the seller.

Pressure range of 0.5 to 10 bar

The published pressure range spans twenty settings. The lowest settings suit tender areas and early sessions, and the upper settings are available where a protocol requires them.

Pressure steps of 0.5 bar

Each adjustment moves the pressure by half a bar. Fine steps let a clinician raise intensity gradually within a session as the patient tolerates it, and record exactly where the session finished.

Pulse frequency of 1 to 21 Hz

Frequency runs across twenty-one settings. Low rates suit focused work on a tender point, and higher rates shorten the time needed to deliver a large shot count across a wider area.

Frequency steps of 1 Hz

Pulse rate changes one hertz at a time. The fine step keeps frequency as reproducible as pressure when a course is documented.

Preset shot count of 100 to 9,900

Set session length before treatment in blocks of 100 shots. The published range covers short sessions on small structures and long sessions over large muscle groups.

8-inch touchscreen

All settings are made on an 8-inch touch display. The screen size leaves room for clear parameter readouts, and the manufacturer publishes no details of stored protocols or interface languages, which should be confirmed.

Seven shockwave probes

The datasheet lists seven probes. Their diameters, materials and intended uses are not published and should be itemised by the seller.

Rated power of 380 W

The unit draws a rated 380 W. That load sits comfortably on a standard clinical wall socket and needs no dedicated circuit.

Supply options of 220 V 50 Hz or 110 V 60 Hz

Both common mains standards are listed. Whether this is one switchable unit or two factory versions is not stated, so the supply is specified at order.

Compact cabinet of 360 × 410 × 305 mm

The published dimensions give a footprint small enough for a bench, a shelf or a mobile trolley beside the couch. The axis order follows the datasheet and should be confirmed against the physical unit.

Unit weight of 18.5 kg

The cabinet weight keeps the unit movable between rooms by one person. The shipped weight of 43 kg is much higher; please confirm the reason from the packing list.

Side-holstered handpieces in photography

Product photography shows two handpieces resting in holsters on the right-hand side of the cabinet. The written specification does not describe the second handpiece, so confirm its supply and function in writing before ordering.

The T606+2 gives a musculoskeletal clinic fine control over pressure, pulse rate, and shot count from one touchscreen, in a cabinet light enough to move between rooms. Its strongest case is in audited treatment of refractory tendon and fascia conditions, where a dose written down as three numbers can be repeated exactly. Its gaps are real and fixable at quotation: no energy flux density, no configuration list, no handpiece service life and an unexplained "+2" suffix. Medigear.uk lists the T606+2 for business buyers worldwide and can arrange delivery, installation, commissioning, familiarisation and service cover. Request the per-probe energy data, handpiece service terms, packing list and declaration of conformity from the seller at quotation.

FAQ

Frequently Asked Questions

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

Radial shockwave units are used in musculoskeletal practice for chronic tendon and fascia problems, most often plantar fasciopathy, lateral elbow pain, Achilles tendinopathy, greater trochanteric pain and calcific shoulder tendinopathy. The manufacturer's datasheet lists parameters and no indications, so the intended purpose stated in the instructions for use governs what the device may be marketed for. The published evidence for these uses is mixed, and the Clinical Applications section below sets out what the trials and NICE guidance actually found. Buyers should read that before building a service around a single indication.

The datasheet does not say. Product photography shows two handpieces holstered on the side of the cabinet, while the written specification describes a single shockwave output with seven probes. The suffix could denote a second handpiece, a second treatment mode or an accessory bundle, and each possibility changes the price and the risk assessment. Ask the seller to state in writing what the suffix means, whether the second handpiece is supplied, what it does and what its published parameters are.

Bar is the driving pressure of the pneumatic generator inside the applicator. The energy that reaches the tissue, usually quoted as energy flux density in mJ/mm², depends on that pressure, the probe fitted, and the manufacturer publishes no energy figures at all. One trial summarised in the NICE evidence overview for calcific shoulder tendinopathy ran its radial arm at 1.5 to 3.0 bar and reported this as 0.01 to 0.35 mJ/mm², which shows how device-specific the conversion is. Request per-probe energy data before matching the unit to any published protocol.

The dominant running cost of a pneumatic shockwave unit is applicator wear, because the internal projectile and guide tube are replaced after a set number of shots. Neither the rated shot life nor the price of a service kit is published for this model. Ask the seller for both, along with the spares lead time and whether servicing can be done on site or requires returning the handpiece to the manufacturer. Coupling gel is a small recurring cost, and electrical safety testing follows the provider's own policy for powered equipment.

The datasheet lists seven probes and gives no diameters, materials or intended uses for them. Probe size affects how energy spreads across the skin, so the list matters for both protocol matching and patient comfort. Request an itemised probe list with diameters and the manufacturer's recommended use for each, and confirm which probes are included in the price and which are sold separately.

An active therapeutic device that delivers energy to the body is typically Class IIa under UK MDR 2002, or higher, use-dependent, and the class is confirmed against the declaration of conformity at order. Great Britain currently accepts CE-marked devices under transitional arrangements running to 2028 or 2030, depending on the EU legislation involved, and the MHRA consulted in 2026 on recognising CE marking indefinitely. UKCA marking remains the alternative route. Because the manufacturer is based outside the UK, a UK Responsible Person and MHRA registration are required before the device is placed on the GB market, so ask the seller who holds that role.

The general medical electrical standard IEC 60601-1 and its electromagnetic compatibility collateral IEC 60601-1-2 are the expected baseline. The particular standard IEC 60601-2-36 covers lithotripsy equipment and other devices using focused pressure pulses, so it does not apply to a radial pneumatic applicator. Ask the seller which standards the manufacturer's technical file cites and for the test reports behind them. The internal air circuit also raises a pressure question: ask for the working pressure and air volume so the duty holder can decide whether the Pressure Systems Safety Regulations 2000 require a written scheme of examination.

Registered clinicians such as physiotherapists and podiatrists regulated by the HCPC normally deliver shockwave therapy, or doctors in sports and musculoskeletal medicine. NICE guidance for plantar fasciitis and Achilles tendinopathy calls for special arrangements covering clinical governance, consent, and audit, assuming a trained operator working within a documented protocol. Staff familiarisation can be arranged at commissioning, but formal competency training remains the provider's responsibility.

It is a poor fit for a buyer who needs published energy flux density figures before committing to a protocol, because none are available until the manufacturer supplies them. It is also a weak choice for a clinic that depends on fast on-site repair and has not agreed on a local service route for the handpiece. For patients, trial exclusion criteria commonly include anticoagulant use, bleeding disorders, pregnancy, local infection and tumours in the treatment area, and the manufacturer's instructions for use set the definitive contraindication list.

The unit is listed for 220 V 50 Hz or 110 V 60 Hz supplies. The datasheet does not say whether this is one switchable unit or two factory versions, so specify the supply at order and confirm the plug type fitted. Rated power is 380 W, which a standard clinical wall socket supports without special wiring.

No standard configuration list is published. The packing weight of 43 kg is more than twice the 18.5 kg unit weight, which suggests accessories, a second handpiece or heavy packaging, and none of these should be assumed. Ask the seller for a written packing list covering handpieces, probes, mains lead, footswitch if any, gel and documentation, and check it against the carton on delivery.