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Texua Physiotherapy & Wellness Equipment

Texua ECT+8

Product Code: PAWE-EAPD-3217

Pick a rate between 1 Hz and 38 Hz on one 10.4-inch touchscreen.

Two magnetic ring applicators share one 800 W tower, sized at 500 × 335 mm across the base so it fits beside a treatment couch. Its natural home is a physiotherapy service that screens every patient before the first session.

Sections

PEMF Therapy

Categories

Physiotherapy & Wellness Equipment

Condition

New

Origin

China

Seller Type

Certified Professional Seller

Size:

500 × 335 × 1025 mm

CE & ISO Certified

Global Shipping

Supplier: Medigear

Texua's ECT+8 is a floor-standing pulsed magnetic therapy unit built by Guangzhou Texua Electronic Technology Co., Ltd., featuring two ring-shaped applicators. The datasheet publishes a 1 Hz to 38 Hz frequency range, a 10 to 100 energy scale in an undefined unit printed as MJ, a 7 T figure listed under energy, an 800 W rating, a 10.4-inch touchscreen and a 220 V/50 Hz or 110 V/60 Hz supply. It states no intended purpose, contraindications, pulse width, waveform, session timer, programmes, cooling method or applicator service life.

What sets the unit apart is the 7 T figure, which marks the rings as strong pulsed-field sources and puts safety first. Every patient needs screening for active implants, metal implants, body-worn devices and pregnancy, and the employer owes staff an exposure assessment under the Control of Electromagnetic Fields at Work Regulations 2016. The Tesla measures magnetic flux density, not energy, and no measurement position or method is given, so both tasks rely on manufacturer data supplied by the seller.

The touchscreen is the only control surface listed; the tower weighs 38 kg, and the 800 W figure is not identified as input or output. Photography shows castors and two ring support arms, but neither appears in the written specification, and no brake is stated. For UK mains, specify the 220 V/50 Hz build with a confirmed 230 V rating and a fitted UK plug.

The unit measures 500 × 335 × 1025 mm and packs to 610 × 610 × 1165 mm at 63 kg. Medigear.uk lists the ECT+8 for UK business buyers. Request the declaration of conformity, instructions for use with contraindications, UK Responsible Person details, MHRA registration evidence, the test method behind the 7 T figure and each ring's service life from the seller before ordering.

Musculoskeletal outpatient physiotherapy is the most natural setting for the ECT+8. A registered physiotherapist assesses the patient, decides whether pulsed magnetic therapy suits the presentation and records the settings used- the same assessment-first route that UK clinics offering high-intensity magnetic therapy describe. Private clinics already running shockwave or other energy-based treatments can add it to those rooms, provided the booking process asks the implant, body-worn device and pregnancy questions before the patient arrives.

Sports injury and club physiotherapy teams use magnetic therapy on tendon, muscle and joint complaints alongside loading programmes. In England, treatment given at a sports ground or gym solely for people taking part in sport sits outside the CQC-regulated activity covering treatment of disease, disorder or injury. The same treatment in a clinic run by listed healthcare professionals generally falls inside it, so the service model decides the registration position.

Orthopaedic and post-operative rehabilitation services can use the unit as one element of an exercise-led programme. NICE's osteoarthritis guideline centres non-drug care on therapeutic exercise, and with trial results on pulsed magnetic fields pointing in different directions, pain services should treat the modality as an adjunct and review outcomes against their own measures.

Employer-run and occupational health clinics carry a second obligation, because operators sit in the field as well as patients. The staff assessment under the Control of Electromagnetic Fields at Work Regulations 2016 needs revisiting whenever an operator declares a pregnancy or an implant.

Independent clinics usually buy direct, while NHS trusts and other public-sector buyers apply their own medical device management checks before equipment of this type enters service. The conformity documentation those procurement routes require is issued by the manufacturer and provided by the seller.

Two Applicators Ready on One Unit

The specification lists two magnetic ring handles, so the tower comes with a second applicator on hand. Whether both can run at once or at independent settings isn't published, and that answer shapes how a service books its rooms.

A Rate Range Protocols Can Work Within

A published span of 1 Hz to 38 Hz gives a clinical lead room to set the rate a chosen protocol calls for. With the rate shown on screen, it is simple to record for every patient, which supports the audit trail a screened service needs.

Settings That Are Easy to Record

A 10.4-inch display keeps the rate and energy level readable, so exact parameters go into the treatment record without guesswork. That matters when outcomes are reviewed against mixed trial evidence.

A Footprint That Leaves Standing Room

The tower takes up 500 × 335 mm of floor space. The space left around the couch does more than ease access, because the staff exposure assessment may ask operators to stand back from the rings while pulses run.

Nothing Listed to Restock

No consumables appear on the datasheet. If the seller confirms the rings need no covers, coolant or specified cleaning products, the unit adds nothing to the regular order list.

Mains Demand Most Rooms Can Meet

An 800 W rating sits well within a UK 13 A socket's capacity, provided the seller confirms it is the input figure. No dedicated supply is listed, so installation centres on a suitable socket and the provider's electrical safety testing.

One Model Across UK and 110 V Sites

The 220 V/50 Hz and 110 V/60 Hz builds let a group with clinics abroad standardise on one model, one protocol and one training package. For UK sites, the 50 Hz build is the one to specify.

A Maker With a Wider Energy-Therapy Line

Guangzhou Texua Electronic Technology lists shockwave, ultrasound, magnetic ring, magnetic slimming and laser therapy devices in its published range. A service buying several energy-based devices from the same maker can take documentation and service questions to a single manufacturer.

Two Magnetic Ring Handles

The datasheet lists the applicators as "Magnetic Ring Handle 2", and the photograph shows two ring-shaped heads. The ring inner diameter is not published, which matters when treating larger knees, shoulders and thighs.

Frequency Range of 1 Hz to 38 Hz

The published range runs from 1 Hz to 38 Hz. The adjustment step, and whether the rate can change mid-session, are not published, and some trial protocols use rates above 38 Hz.

Energy Level Scale of 10 to 100

Output is set on a scale published as 10 to 100, with the unit printed as MJ. Nothing on the sheet defines that unit, so the numbers work as a relative scale until the seller says otherwise.

Published 7 T Figure

The sheet lists 7 T under the heading Energy. A tesla measures magnetic flux density, and the figure arrives without a measurement position, distance or method.

800 W Power Rating

The power figure is 800 W, but it doesn't state whether it refers to mains input or magnetic output.

10.4-Inch Touchscreen

The touchscreen is the only interface listed. The datasheet does not say whether the software stores protocols, logs sessions or offers English-language menus, so ask for screenshots or a demonstration.

Dual-Voltage Supply Options

The ECT+8 is offered for 220 V/50 Hz or 110 V/60 Hz mains. UK services need the 50 Hz build confirmed for the 230 V supply, with a UK plug fitted.

Upright Tower Format

The body measures 500 × 335 mm at the base and stands 1025 mm high. Whether that height includes any ring support arms is not stated.

38 kg Unit Weight

At 38 kg, the tower needs a manual-handling assessment before moving between floors or buildings.

Packing Size and Weight

The shipment weighs 63 kg. Packing dimensions are published as 61 × 61 × 116.5 with the unit printed as mm, which cannot be right because the unit itself is larger, so they read as 610 × 610 × 1165 mm and about 0.43 m³.

Arms and Castors Shown in Photography

The photograph shows each ring on a support arm and the tower on castors. Neither appears in the written specification, and arm reach, arm locking and castor brakes are not published, so ask for the full standard supply on the quotation.

Pulse Parameters to Confirm

Pulse width, waveform, burst pattern and session timing are not published. They decide whether a published trial protocol can be reproduced on the unit.

Cooling and Ring Service Life to Confirm

No cooling method or applicator service life is published. Ask how the rings are cooled, how many pulses or hours each is rated for, and how quickly a replacement arrives.

The ECT+8 packs two magnetic ring handles, rates from 1 Hz to 38 Hz and a 10.4-inch touchscreen into an upright tower. How well it serves a physiotherapy service depends on the documents that travel with it. The 7 T figure needs its test method, the energy scale needs a definition, and the contraindications, exposure data and ring service life all need to be in writing before the first session is booked. Services that screen every patient and assess their own staff exposure are best placed to use it. Medigear.uk lists the ECT+8 for UK business buyers and can arrange delivery, installation, commissioning, familiarisation and service cover. Request the instructions for use, the declaration of conformity, UK Responsible Person details and MHRA registration evidence from the seller at quotation.

FAQ

Frequently Asked Questions

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

It delivers pulsed magnetic fields through two ring-shaped applicators, with the rate adjustable from 1 Hz to 38 Hz and energy set from 10 to 100 via the 10.4-inch touchscreen. Pulse width, waveform, timer range and preset programmes are not published. The treatment protocol therefore has to come from the manufacturer's instructions for use, which the seller should supply before planning any clinical session.

The sheet lists 7 T under the heading Energy, but the tesla is a unit of magnetic flux density. No measurement position is given, and field strength falls away quickly with distance from a coil, so the figure could describe the ring surface, the ring centre or a point further out. Ask the seller for the manufacturer's test method and report before the figure appears in patient information or the staff exposure assessment.

The datasheet prints the unit as MJ without defining it, and megajoules would be implausible for a handheld ring. Treat the numbers as a relative scale until the seller confirms whether each step is a percentage of maximum output or a measured energy value. Protocols written around the scale only transfer between units once that definition is in writing.

No contraindications are published, so the complete list must come from the manufacturer's instructions for use. UK clinics offering high-intensity magnetic therapy typically exclude people with pacemakers and anyone who is pregnant. Active implants, metal implants and body-worn devices such as insulin pumps are the usual screening questions for strong pulsed fields, and use over the head should be ruled out unless the instructions say otherwise. Build those questions into the booking form so they are asked every time.

The Control of Electromagnetic Fields at Work Regulations 2016 require employers to assess the electromagnetic fields their employees may be exposed to. Staff with implanted or body-worn medical devices, and pregnant staff, count as being at particular risk and need specific consideration. HSE's guide HSG281 explains how to carry out and record the assessment. The datasheet gives no field data at operator positions, so request it through the seller and use it to decide where staff stand while pulses run.

It points in different directions. A 2022 meta-analysis of 11 randomised trials in osteoarthritis reported gains in pain, stiffness and physical function, while a 2019 meta-analysis of knee osteoarthritis trials found better physical function but no advantage for pain or stiffness. A 2026 review of knee trials found no significant change in pain or overall function scores at one month, with a pain benefit at 18 to 21 days that did not last. Trial devices varied widely in field strength and frequency, so these results cannot be assumed to carry over to this unit's settings. NICE's osteoarthritis guideline centres non-drug care on therapeutic exercise and advises against several electrotherapies, including pulsed short-wave therapy, on insufficient evidence of benefit.

If the manufacturer's intended purpose is therapeutic, as the product category suggests, the unit falls under the UK Medical Devices Regulations 2002, typically as Class IIa or higher depending on use, as the declaration of conformity will state. A non-UK manufacturer must appoint a UK Responsible Person, who registers the device with the MHRA before it reaches the Great Britain market, and registration is a listing, not an approval. The electrical safety reference is IEC/BS EN 60601-1 with the IEC 60601-1-2 collateral for electromagnetic compatibility, while the nearest particular standard, IEC 60601-2-10, is written for electrical nerve and muscle stimulators, so ask which standards were applied. No CE mark appears on the supplied datasheet, and Great Britain currently accepts CE-marked devices under transitional arrangements that the MHRA consulted on extending in 2026.

It suits musculoskeletal and sports rehabilitation services led by registered physiotherapists who assess each patient first and use magnetic therapy alongside exercise. It is a poor fit for any service that needs published contraindications, exposure data and conformity documents before raising an order, because the datasheet carries none of them. Home use, aesthetic body-contouring work and any treatment over the head fall outside what the datasheet describes. Where a fully documented specification is needed at the point of enquiry, Medigear.uk can point the buyer to an alternative specification.

It runs on 220 V/50 Hz or 110 V/60 Hz mains with an 800 W rating, which a UK 13 A socket carries comfortably if that is the input figure. Ask for the 50 Hz build with a UK plug and written confirmation of its 230 V rating. As powered medical electrical equipment, it falls under the provider's electrical safety testing schedule, and PUWER 1998 covers its maintenance, suitability, and operator training. At 38 kg, moving between floors requires a lift or a manual handling assessment.

No cooling method, applicator service life or service interval is published. Ring applicators driven at high output generate heat, so ask how each ring is cooled, how long it can run before resting, how many pulses or hours it is rated for, and how quickly a replacement arrives. The seller sets warranty terms in the quotation, and Medigear.uk can arrange delivery, installation, commissioning, staff familiarisation, and service cover.

In UK clinical shorthand, ECT means electroconvulsive therapy, which has no connection with this device. A referral or asset record that shortens the name could be misread by colleagues outside the physiotherapy team. Record the full product name and describe the modality as pulsed magnetic therapy in referral letters, consent forms and the equipment register.