Sale on Manual & Electric Hospital Beds - Starting from 25 September!

MediGear Group Limited
B2B
  1. Home
  2. Shop
  3. Orthopaedic, Trauma & Prosthetics
  4. Aulexmed BL-52014-A
✓ Certified Professional Seller Aulexmed BL-52014-A
Aulexmed BL-52014-A
Aulexmed BL-52014-A
Aulexmed BL-52014-A
Aulexmed BL-52014-A
Aulexmed Orthopaedic, Trauma & Prosthetics

Aulexmed BL-52014-A

Product Code: OTAP-OBAS-3535

The only test this boot requires is a look at the skin.

Paperwork for this tall grey walker boot stays short. No electrical parts to test; two air cells fed by a built-in pump set the fit, and a washable liner with an open toe keeps skin checks simple over weeks of wear.

Sections
Ankle & Foot Orthoses
Categories
Orthopaedic, Trauma & Prosthetics
Condition
New
Origin
China
Seller Type
Certified Professional Seller
CE & ISO Certified
Global Shipping
Supplier: Medigear
Share: Facebook LinkedIn Twitter Pinterest

Tall, grey and pneumatic, Aulexmed's BL-52014-A is a walker boot for fracture clinics, orthopaedic surgery and emergency departments. The datasheet lists a built-in air pump with pressure adjustment, dual airbags for compression and fit, an open toe described as lightweight and breathable, a detachable washable inner lining, and a shell for either the left or the right foot. Four sizes are listed, S to XL, and the colour is grey. Shaft height, weight, sole profile, ankle angle and materials are not published.

Governance is where this boot asks little and where the page is most useful. With no electrical parts, it sits outside electrical safety testing entirely, and there is nothing to charge or service. What it does bring is the documentation every lower limb device brings: a declaration of conformity naming the legal manufacturer, evidence that the device has been registered with the MHRA through a UK Responsible Person, and, at the point of issue, the VTE risk assessment that NICE expects for adults discharged with an immobilised leg. None of these appears on the supplied sheet, and all should be in hand before the first patient is fitted.

Product photography shows a tall grey shell with pale grey straps spaced along its length and a dark sole. The integral pump fills the two air cells and releases them through the adjustment system, so the fit can follow swelling as it falls.

The size table runs from S, a 10.6 in insole for shoe sizes 35 to 39, to XL, a 13.8 in insole for sizes above 46. No dimensions are given. Medigear.uk lists the BL-52014-A for business buyers worldwide; request the declaration of conformity, the UK Responsible Person details, the instructions for use and the shaft height from the seller before ordering.

Fracture clinics are the obvious home for the BL-52014-A, and also where its documentation load shows up. A stable ankle fracture managed in a removable device can be fitted at the first appointment, with the tall shell holding the lower leg along its length and the air cells taken up as swelling falls. The fitting record, VTE assessment, and patient leaflet complete the episode.

Orthopaedic and foot and ankle surgical units can issue it for protection after ankle surgery, including fracture fixation and ligament repair where the surgeon wants the whole lower leg held. Theatre and ward teams will want the instructions for use on file before the first patient goes home in one.

Emergency departments and minor injury units may stock it for ankle fractures and ligament injuries under a clinician's direction. The boot meets RCEM's audit standards on VTE in lower limb immobilisation, which require a documented risk assessment, a patient leaflet, and a first dose of any prescribed prophylaxis before the patient leaves.

Physiotherapy services continue care as patients start weaning out of the boot. The washable liner and open toe help with the skin care that runs through that stage.

Procurement and medical device governance teams carry the rest. Before listing the boot on a formulary, they will want the declaration of conformity, the UK Responsible Person and registration details, and written answers on reuse and heel wedges. NHS procurement routes ask for exactly that pack, and equivalent public procurement elsewhere asks for its own version. The conformity documentation those procurement routes require is issued by the manufacturer and provided by the seller.

No electrical testing to schedule

The boot has no electrical parts. It never appears on a portable appliance testing list and needs no charging or servicing.

A documentation pack that is easy to define

Declaration of conformity, UK Responsible Person details, registration evidence and instructions for use cover the device side. A governance team can list what it needs before the first order.

Mechanical inflation built in.

The pump is part of the boot, so there is no separate device to track, clean or replace. Air is added and released through the listed adjustment system.

Lower leg held along its length.

The tall shell reaches well up the leg in photography. That suits injuries where the clinician wants control above the ankle.

Skin checks are straightforward.

An open toe and a detachable, washable liner make daily skin and circulation checks practical for patients and carers.

One design for either foot

The shell fits the left or the right foot. Four stock lines cover the range, one per size.

Four sizes from 35 upward

Sizes S to XL cover shoe sizes 35 to above 46. Large adult feet are included in the range.

A neutral grey finish

Grey is the listed colour. It suits patients returning to work or public settings.

Tall shell

Product photography shows a shell reaching well up the lower leg. The height is not published.

Built-in air pump

A mechanical pump integrated into the boot fills the air cells. Its exact position is not stated.

Pressure adjustment system

Air can be added and released through the listed system. No pressure indicator is described.

Dual airbag design

Two air cells are listed for compression and fit. Their placement within the tall shell is not given.

Full-length strapping

Pale grey straps are spaced along the shell in photography. Strap count and fastening type are not stated in writing.

Open-toe design

The forefoot is open at the front. That supports ventilation, dressings and toe checks.

Lightweight and breathable

The manufacturer describes the construction as lightweight and breathable. No weight or materials are published.

Detachable inner lining

The lining lifts out of the shell. This allows separate washing and drying.

Washable liner

The liner is listed as washable. Care instructions should be requested.

Universal left and right fit.

One shell design serves either foot. The same size fits a left or a right injury.

Four sizes

Sizes S to XL run from a 10.6 in to a 13.8 in insole. Shoe sizes run from 35 up to 46.

Grey finish

The boot is listed in grey. The photos show a pale grey shell and straps with a darker sole.

No electrical components

The boot contains nothing powered. No electrical safety standard applies.

The BL-52014-A keeps its demands on a service modest. There is nothing electrical to test; the pump is built in, and a washable liner with an open toe keeps skin checks practical through weeks of wear, all in a tall grey shell that fits either foot across four sizes. The work is in documentation, and the supplied sheet doesn't include it. Medigear.uk lists the BL-52014-A for business buyers worldwide and can arrange delivery and quotations. Request the declaration of conformity, the UK Responsible Person and registration details, the instructions for use, the shaft height, and the heel wedge position from the seller with the quotation.

FAQ

Frequently Asked Questions

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

Ask the seller for the declaration of conformity, which names the legal manufacturer, the device class and the standards applied, together with the instructions for use and a sample of the labelling. A walker boot of this type is typically Class I under UK MDR 2002, confirmed against the declaration at order. The manufacturer's website also uses the name Benli Medical, so check the legal manufacturer on the declaration against the name on the label. Conformity requirements differ by destination market, and the seller confirms what applies where the boot is going.

Under UK MDR 2002, the MHRA must be informed before a device is placed on the market in Great Britain, including Class I devices. A manufacturer based outside the UK must appoint a single UK Responsible Person to take responsibility for its devices, including registration. Distributors and suppliers do not register themselves. Ask the seller for the UK Responsible Person's name and evidence of registration, since both sit with the manufacturer's side of the supply chain.

Neither mark appears on the supplied datasheet, so do not assume either is held. Great Britain currently accepts CE-marked devices under transitional arrangements that the MHRA consulted on extending in 2026, with UKCA as the domestic route. Northern Ireland follows different rules. Request the marking evidence alongside the declaration of conformity.

No. The boot has no electrical parts, so no electrical safety standard applies and it never enters a portable appliance testing schedule. The pump is mechanical and built into the boot. The recurring checks it does need are clinical, chiefly the skin under the shell and circulation in the toes.

For adults aged 16 and over discharged with lower limb immobilisation, NICE quality standard QS201 expects a documented VTE risk assessment in line with NG89, with verbal and written information for the patient. Services usually also record the size issued, the fitting, and the advice given on skin checks and inflation. Keeping the device's lot or batch details where the labelling provides them allows the service to respond if a field safety notice is ever issued. That documentation belongs to the provider, regardless of the device chosen.

The supplier sheet titles the product as a knee walker boot and includes a trade name that does not belong to Aulexmed. The item is a walking boot for the foot and lower leg, with no wheels and no knee platform. Ask the seller to confirm the product name and trade name that appear on the labelling and the declaration of conformity, so the records match the device on the shelf.

The manufacturer publishes no shaft height. Product photography shows a tall shell reaching well up the leg. Ask the seller for the height in millimetres for each size, and check that the upper edge clears the back of the knee on shorter patients within a size.

Achilles tendon injury and post-operative protection are listed, but the sheet shows no heel wedges or adjustable ankle angle. Achilles protocols typically hold the foot pointing down in the early weeks and bring it up in stages, which in a boot usually depends on wedges. Ask the seller how the indication is meant to be met before adding the boot to an Achilles protocol.

S covers shoe sizes 35 to 39 with a 10.6 in insole, M covers 40 to 43 with 11.0 in, L covers 44 to 46 with 12.6 in, and XL covers sizes above 46 with 13.8 in. The shoe size system is not stated and appears to be EU numbering. The small step from S to M set against the larger step from M to L is worth confirming with the seller. Calf circumference limits are not published, which matters on a tall shell.

The datasheet is silent on reuse. The liner is washable, but no cleaning method is published for the shell, straps or air cells. Treat the boot as a single-patient issue unless the manufacturer's instructions for use state otherwise, and do not start a reissue scheme without them.

It is a poor fit for early-stage Achilles protocols unless heel wedges are confirmed. Patients with reduced foot sensation need close skin surveillance, and no offloading insert is listed for diabetic foot ulcers. Forefoot and toe injuries rarely need a shell this tall. Patients who cannot manage the pump or report numbness and pain need a carer or a different device.