Professional clinic equipment · MDL 114257 DioLaz Diode Laser

A triple-wavelength platform for your clinic.

Review the equipment, handpiece interface and implementation requirements in one place. Built around 755 / 808 / 1064 nm delivery, adjustable output and sapphire contact cooling.

DioLaz diode laser console and handpiece, front product view
Product-gallery image. Confirm the model and handpiece configuration in your quotation.
1,200 W Peak optical output
1–100 J/cm² Adjustable fluence
12 × 24 mm Treatment spot
Approx. −32 °C Minimum sapphire-tip temperature*
Health Canada licensed · Class III · MDL 114257

Licence holder / manufacturer: DioLaz Canada Inc. Review the official record for current status.

Verify Licence ↗
Full-length DioLaz diode laser console on its wheeled base
Full console view for equipment review. Confirm dimensions, weight and clearance requirements with DioLaz.
01 / System overview

Evaluate the platform. Confirm the configuration.

A purchasing overview for clinic owners, procurement teams and qualified operators—not a substitute for the User Manual or a configuration-specific quotation.

01

Technical comparison

Compare wavelength delivery, fluence, repetition rate, pulse duration and cooling specifications against your clinic’s requirements.

02

Defined scope of supply

Confirm the console, handpiece, accessories and services in the quotation. Gallery photos are not a packing list.

03

Implementation planning

Review site readiness, operator training, service arrangements and applicable purchase policies before order approval.

02 / Handpiece interface

Inspect the treatment head and integrated display.

Recent product-gallery views show the contact end and a touch-screen handpiece interface. Match the ordered handpiece to the selected configuration and quotation.

Front and side of the DioLaz handpiece with its contact window
Contact end

Handpiece front view

Review the contact window and handpiece form factor as part of a product demonstration.

DioLaz handpiece with integrated display showing an illustrative interface
Display interface

Built-in touch screen

The close-up shows the handpiece display. Values shown in the photograph are illustrative, not recommended treatment settings.

Model years and availability are controlled by the product selector and confirmed quotation. Different handpieces are not automatically included together.

DioLaz console display, key switch and emergency stop control
Console display and physical controls. This image is not a demonstration of the SHR or HR software screens.
03 / Platform & workflow

Three wavelengths. Two operating workflows.

Combined diode delivery at 755, 808 and 1064 nm, with SHR and HR workflows for professionally assessed treatment plans.

755 nm 808 nm 1064 nm

SHR / In-motion workflow

Continuous movement for broader treatment zones. Use must follow operator training and the applicable protocol.

HR / Targeted pulse workflow

Pulse placement for focused treatment zones. Parameter selection and technique must follow the User Manual.

Treatment suitability, including Fitzpatrick skin types I–VI, requires individual assessment. Published ranges are not a clinical protocol.

04 / Contact & safety interfaces

Inspect the details that support daily operation.

Match each function to its actual component, then confirm installation, compatibility and operator requirements with DioLaz.

DioLaz precision light guide attachment with a curved transparent tip
Precision accessory

Precision light guide

Curved light-guide attachment for small or contoured areas. Confirm compatibility and included accessories for the ordered handpiece.

Close-up of the rectangular contact window on the DioLaz handpiece
Contact cooling

Sapphire contact window

The brochure specifies sapphire-tip cooling down to approximately −32 °C. This is a tip specification—not a target skin temperature.

Rear connectors labelled Foot Switch and Interlocking Device on the DioLaz console
Safety connection

Treatment-room interlock

The rear interface is labelled for an interlocking device. Verify the treatment-room connection and safety checks during commissioning.

05 / Installation & accessories

Plan the room, service access and accessory requirements.

Additional gallery details support pre-installation discussions. Final supplied items and quantities must be listed in the quotation or packing list.

Rear view of the DioLaz console showing ventilation and service connections
Rear console

Ventilation & service access

Confirm rear clearance, access and installation requirements for the supplied unit.

DioLaz rear water inlet, level indicator and outlet labels
Water system

Fill port & level indicator

Follow the current User Manual for water specifications, inspection and maintenance intervals.

Orange guarded foot switch shown in the DioLaz product gallery
Foot control

Guarded foot switch

Confirm the supplied foot control, connection and intended use for your configuration.

Protective eyewear and cases shown in the DioLaz product gallery
Protective equipment

Eyewear & cases

Confirm included eyewear, wavelength coverage and protection specifications before clinical use.

Photos alone do not establish electrical requirements, eyewear certification, interlock commissioning or the complete scope of supply.

06 / Procurement reference

Technical, regulatory & implementation information

Reference data for your equipment comparison and procurement file. All four sections are expanded initially; each can still be collapsed individually.

Order confirmation: The selected model, handpiece, accessories, delivery, training, warranty and commercial terms must be confirmed in the quotation, order documents and applicable policies.

01 Regulatory & supplier record Identification for procurement and compliance review

Regulator: Health Canada

Medical Device Licence: No. 114257

Device class: Class III

Licence type: System

Licence holder / manufacturer: DioLaz Canada Inc.

First issue date: 2025-10-31

Official licence name: DIODE LASER THERAPY SYSTEMS

Current status: Consult the live MDALL record

02 System performance specifications Manufacturer reference values for equipment comparison

Wavelengths: 755 / 808 / 1064 nm

Peak optical output: Up to 1,200 W

Fluence: 1–100 J/cm²

Repetition rate: Up to 10 Hz

Treatment spot: 12 × 24 mm · 2.88 cm²

Pulse duration: 5–300 ms

Beam profile: Uniform top-hat

Sapphire-tip cooling: Down to approximately −32 °C

Reference values reflect the published DioLaz brochure. Confirm specifications for the ordered configuration. Optical output is not the electrical input rating. *Tip temperature is not a skin-temperature target; clinical settings must follow the User Manual.

03 Operator workflow & implementation Training, documentation and commissioning review
01

Operator preparation

Confirm training arrangements, qualified users and access to the current DioLaz User Manual before clinical use.

02

Clinical documentation

Document client assessment, treatment suitability, selected parameters and treatment endpoints in accordance with the applicable protocol.

03

Site & safety checks

Confirm room access, electrical requirements, interlock installation, emergency controls and local laser-safety procedures before commissioning.

04 Scope of supply & commercial review Confirm before purchase approval

Configuration: Selected console, model, handpiece and compatible accessories.

Supply & documentation: Included items, quantities, User Manual and configuration-specific technical information.

Implementation & support: Installation responsibilities, training arrangements, service contact and warranty terms.

Purchase route: Order placement, financing or trial eligibility, delivery and return conditions under the applicable policies.

Discuss your clinic’s equipment requirements.

Share your preferred configuration, clinic location and purchase timeline. Request a configuration-specific quotation and confirm the relevant programs and policies.

For professional use only. Review contraindications, precautions, safety requirements and treatment parameters in the DioLaz User Manual before clinical use.