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Texua Physiotherapy & Wellness Equipment

Texua T805

Product Code: PAWE-EAPD-3524

Every setting moves in fixed steps, so next week's session matches this week's.

Half-bar pressure steps from 0.5 to 10 bar, frequency from 1 to 21 Hz, and an impulse count set in hundreds give each treatment course a written, repeatable recipe. Nine transmitters share one handle on a castored stand.

Sections

Shockwave Therapy

Categories

Physiotherapy & Wellness Equipment

Condition

New

Origin

China

Seller Type

Certified Professional Seller

Size:

570 × 550 × 975 mm

CE & ISO Certified

Global Shipping

Supplier: Medigear

Texua's T805 is a floor-standing shockwave therapy unit designed around stepped control of a single treatment handle. Published figures range from 0.5 to 10 bar in 0.5-bar steps, 1 to 21 Hz in 1 Hz steps, and 100 to 9,900 impulses in steps of 100, all set on an 8-inch touch screen. Rated power is 420 W, with builds for 220 V 50 Hz or 110 V 60 Hz supplies. The standard set is one handle and nine transmitter heads. No second handle, imaging, energy flux density figure or stored protocol library is listed.

The unit is best matched to targets near the surface. Texua lists the T805 as pneumatic and ballistic, and a NICE procedure overview notes that in radial shockwave therapy the peak pressure sits at the skin and spreads as it travels deeper. That suits the plantar fascia, the common extensor origin, the patellar and Achilles tendons, and trigger points a clinician can find by touch. Deep targets suit it poorly, so raise any such caseload with the seller before ordering.

The photographed console stands on a four-caster base, with the screen at the top and a side holder for the handle. It weighs 23 kg. The nine transmitters fit the one handle, and their diameters, shapes and materials are not published. No gel, spare projectiles or tools are listed.

It measures 570 × 550 × 975 mm and packs to 610 × 610 × 1120 mm. It joins the provider's electrical safety testing schedule, and the handle is the main upkeep item, since ballistic handles typically wear their projectile and guide tube with use. Medigear.uk lists the T805 and can arrange delivery and commissioning. Before ordering, request the declaration of conformity, the handle service interval in impulses, the instructions for use, and the noise level from the seller.

Musculoskeletal physiotherapy outpatients are the natural home for the T805, alongside sports medicine clinics, podiatry and foot health services, orthopaedic outpatient departments and club medical rooms. The common thread is a caseload of chronic, superficial soft-tissue problems that have not settled with exercise and load management.

Refractory plantar heel pain is the indication most buyers will start with. In the UK, NICE allows ESWT only with special arrangements for governance, consent, and audit or research, because trial results have been inconsistent; the same applies to Achilles tendinopathy. Lateral elbow tendinopathy, patellar tendinopathy and myofascial trigger points are frequent targets in outpatient practice, and each sits close enough to the skin for a radial pressure wave to reach. For the shoulder, a 2025 guideline in the Journal of Orthopaedic and Sports Physical Therapy supports shockwave therapy when the rotator cuff tendon is calcified and advises against it when it is not, making imaging a prerequisite for that caseload even though the console has none.

The radial protocols cited on this page ran weekly sessions of around 2,000 impulses at low pressures, and the T805's counter and frequency range cover that pattern. Texua also lists urology among the fields for this device, but any service considering that use should examine the evidence and regulatory position for it on its own terms.

Where the unit enters a structured service, the impulse count and settings for each session belong in the patient record, since that is the audit trail NICE expects. NHS procurement routes ask for device class, conformity evidence and electrical safety documentation, and equivalent public procurement elsewhere asks the same. The conformity documentation those procurement routes require is issued by the manufacturer and provided by the seller.

A course of treatment that can be written down

Pressure in 0.5-bar steps, frequency in 1 Hz steps, and impulses in hundreds turn each session into three plain numbers. A clinician covering a colleague's list can read the record and deliver the same settings without guesswork, which matters for a therapy given over several weekly visits.

A frequency range that spans published protocols

The radial trials cited on this page ran at frequencies between 5 and 15 Hz. The T805 covers 1 to 21 Hz, so a service can follow those protocols and still lower the rate for a patient who finds a session hard to tolerate.

One handle for the whole team to learn

A single handle and one touch screen keep training short for rotating staff. Every clinician works the same controls, and one in-service session covers the whole device.

Nine transmitter heads in the standard set

The nine heads arrive with the console as part of the standard set. Their sizes and profiles are not published, so ask for the list before deciding whether it covers the service's caseload.

Easy to move between treatment rooms

At 23 kg on a castored base, the console can be wheeled between cubicles or taken to a clinic room for a single session. A department sharing one unit across several clinicians gains the most from this.

A supply build for the destination

The unit is offered for 220 V 50 Hz or 110 V 60 Hz supplies. Buyers can specify the build that matches their mains when ordering, and should confirm the plug type at the same time.

No radiation or laser duties

Nothing on the T805 emits ionising radiation or laser light. No Radiation Protection Adviser or Laser Protection Adviser is needed,leavings electrical safety testing, PUWE,R and any pressure-system check as the main obligations.

A counter that supports audit

Because the impulse count is set before each session, the number delivered is known and can be recorded. Services running under NICE special arrangements need exactly that kind of consistent record for outcome audit.

Honest scope from the start

The T805 is built for targets a clinician can locate by touch. Buying it on that understanding keeps expectations realistic for the service, the clinicians and the patients who will be treated with it.

Stepped pressure control

Output runs from 0.5 to 10 bar in 0.5-bar steps. This is the air pressure driving the projectile, and it should not be read as energy delivered to tissue.

Adjustable frequency

Pulse frequency is adjustable from 1 to 21 Hz in single-hertz steps. Trial protocols have lowered the rate in response to patient discomfort.

Preset impulse count

A target impulse count is set between 100 and 9,900 in steps of 100. That range spans the per-session counts used in the published radial protocols cited on this page.

8-inch touch screen

All settings are made on an 8-inch touch screen at the top of the console. The datasheet does not describe the software, language options or any stored protocols.

Pneumatic ballistic drive

Texua lists the T805 as a pneumatic, ballistic device. The datasheet itself does not state the drive, so confirm the arrangement and the source of compressed air with the seller.

Nine transmitter heads

Nine transmitters are supplied as standard. Diameters, profiles and materials are not published, and replacement availability should be confirmed before order.

Single shockwave handle

One handle carries every transmitter. Its service interval in impulses is not published and is the key upkeep figure to request.

Handle holder

The photographs show a holder on the side of the console where the handle and its hose rest between patients. Confirm that the holder is part of the standard build.

Castored floor stand

The console sits on a four-caster base for movement between rooms. The datasheet does not describe castor braking.

Rated power

Rated power is 420 W. The datasheet does not say whether this is the input rating or a peak figure.

Supply options

The unit is offered for 220 V 50 Hz or 110 V 60 Hz. Specify the destination supply at order.

Compact footprint

The console measures 570 × 550 mm at the base and stands 975 mm tall. Check the space beside the treatment couch against that footprint before delivery.

Console weight

The console weighs 23 kg. Packed, the consignment reaches 47.6 kg.

Panel marking

The photographed side panel carries the marking "Shock Wave Tplus+" and the Texua logo. Buyers who need neutral or own-brand panels should ask the seller before ordering.

Chinese manufacture

Guangzhou Texua Electronic Technology Co., Ltd. in Guangdong makes the T805. The seller sets warranty terms, spare parts routes and service arrangements in the quotation.

The T805 gives physiotherapy, podiatry, or sports medicine services a stepped, repeatable way to deliver shockwave therapy to superficial tendons and fascia. Its strengths are simple ones. Every setting moves in fixed steps, the impulse count is known before each session begins, and one handle serves the whole team. Its limits are just as clear. The datasheet publishes no energy flux density, no handle service interval and no conformity marking, and the pressure wave peaks at the skin. Buyers who plan around those facts will get a dependable outpatient tool. Medigear.uk lists the T805 for business buyers worldwide and can arrange delivery, installation, commissioning, familiarisation and service cover. Request the declaration of conformity, the IEC 60601 test reports, the handle service interval and the instructions for use from the seller at quotation.

FAQ

Frequently Asked Questions

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

Texua describes the T805 as pneumatic and ballistic: compressed air drives a small projectile against the transmitter, which sends a pressure pulse into the tissue. Pulses from this kind of source spread outward from the transmitter tip, and the highest pressure is at the skin. Physicists usually call them radial pressure waves, and some reviewers argue the label matters when reading trial reports. The datasheet does not say whether any of the nine transmitters shapes the wave differently, so ask the seller for the transmitter specifications.

Not necessarily. Bar describes the air pressure driving the projectile, while energy reaching tissue is normally expressed as energy flux density in mJ/mm², and the link between the two depends on the device and the transmitter. Texua does not publish an energy flux density figure for the T805. In one sham-controlled trial summarised by NICE, radial treatment ran between 1.5 and 3.0 bar and was reported as 0.01 to 0.35 mJ/mm², placing that protocol toward the lower end of this unit's range. IEC 63045:2020 describes how acoustic output from pressure-pulse devices, ballistic generators included, should be measured, so ask the seller whether any such data exists for this model.

The picture is mixed and depends on the condition. In the UK, NICE guidance on refractory plantar fasciitis (IPG311, 2009) found no major safety concerns but inconsistent evidence of efficacy, and recommends use only with special arrangements for clinical governance, consent and audit or research. NICE reached a similar position on Achilles tendinopathy in 2016, in guidance now published as HTG426. A 2025 clinical practice guideline in the Journal of Orthopaedic and Sports Physical Therapy supports considering shockwave therapy for calcific rotator cuff tendinopathy but advises against it where no calcification is present. A service built around this unit should plan an outcome audit from the first patient.

Services whose main caseload lies deep beneath a thick muscle layer will get little from a pressure wave that peaks at the skin. It is also a poor fit for teams that want image-guided targeting built into the console, because none is listed. Texua mentions urology among its intended fields, but this page makes no claim for erectile dysfunction or aesthetic uses, and buyers interested in those should review the evidence and regulatory position separately. Clinicians who need to reproduce a published protocol at an intermediate setting such as 2.2 bar will find that the half-bar step lands either side of it.

On ballistic devices, the projectile and guide tube inside the handle wear with every impulse, and handles are usually serviced or rebuilt after a stated number of shots. Texua does not publish that number for the T805, and it is the most useful single figure to obtain before order. Transmitter heads can also wear or chip at the contact face over time. Ask the seller for the service interval in impulses, the turnaround for a handle rebuild and whether spare projectiles and transmitters are held in stock.

The datasheet lists 220 V 50 Hz or 110 V 60 Hz, which suggests a choice of two supply configurations. It does not state that a single unit accepts both. Specify the destination supply when ordering and confirm the plug type fitted. Check with the manufacturer before running the unit through any transformer, since that can affect the electrical safety basis of medical electrical equipment.

In the UK, a therapeutic device of this kind is typically Class IIa under UK MDR 2002, or higher depending on intended use, confirmed against the declaration of conformity at order. No CE or UKCA marking appears on the T805 datasheet, and marketplace listings for the range refer to Chinese domestic certification, which does not establish UK or EU conformity. Request the declaration of conformity, the certificate scope, the IEC 60601-1 and IEC 60601-1-2 test reports for this model and the instructions for use. Conformity requirements differ by destination market, and the seller confirms what applies where the unit is going.

Texua positions the device for orthopaedics, physiotherapy, sports medicine and urology. In the UK, the clinicians most likely to use it, physiotherapists and podiatrists, are regulated by the HCPC, and doctors by the GMC. Provider registration depends on the UK nation and the services offered. Where a treatment falls under NICE special arrangements, the provider needs governance sign-off, documented consent and outcome audit in place before the first session.

The 420 W rating and the bar-scaled output point to an air supply inside the console, but the datasheet gives no compressor or reservoir details. In the UK, whether the Pressure Systems Safety Regulations 2000 require a written scheme of examination depends on the system's pressure and volume. Ask the seller how the air is generated and stored, and what the manufacturer states about PSSR.

The published standard configuration is the console, one shockwave handle and nine transmitter heads. Coupling gel, spare projectiles, a handle rebuild kit and a dust cover are not listed. The photographs show the handle resting in a side holder, but confirm every accessory in writing with the quotation. The 47.6 kg packed weight is worth passing to the goods-in team ahead of delivery.

Each session is set by pressure, frequency and a target impulse count between 100 and 9,900. The fixed steps make a session easy to write into the treatment record and repeat at the next visit. The datasheet does not say whether the unit stores user protocols or logs delivered impulses, so the clinical record remains the audit trail. That matters wherever NICE special arrangements ask for outcome audit.