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DioLaz Health Canada Licensed Fractional CO2 Laser Skin Resurfacing Machine
Review the official MDALL record for the listed system and manufacturer before purchase.
Medical device licence:
MDL 114258
Classification:
Class III · System
Manufacturer:
DioLaz Canada Inc.
Official MDALL record · Opens in a new tab
A 10,600 nm platform for clinics evaluating fractional resurfacing and focused delivery. Compare the handpieces, review operating requirements and confirm the complete order package with DioLaz.
One resource directory for programs, warranty, training, shipping, returns and support. Website links open in a new tab.
View full-size image↗ Review the current product options, then confirm the selected model and handpiece separately in the written quotation.
View full-size image↗ Use the current product selector for the model designation. Confirm availability and the applicable specification sheet before payment.
Choose between traditional and built-in touchscreen handpiece options. Confirm model compatibility, controls and the items included in your quotation.
Ask for an itemized quotation covering the console, handpieces, accessories, training, delivery and any optional services.
Photographs illustrate the platform and its components; they do not establish the contents of every order.
Evaluate each delivery component against the planned procedures, operator qualifications and device-specific instructions.
View full-size image↗ Workflow: Patterned micro-spot delivery with adjustable scanning parameters for professional resurfacing.
Before ordering: Confirm the selected model, applicable settings and fractional handpiece specification.
View full-size image↗ Workflow: Focused delivery for selected cutting, ablation and coagulation procedures.
Before use: Confirm device instructions, operator qualifications and authorized professional scope.
View full-size image↗ Workflow: A dedicated probe configuration for procedure-specific applications.
Before ordering: Confirm compatibility, authorized uses and training; the photo is not an authorization.
View full-size image↗ The console features a 12.1-inch colour touchscreen, programmable presets and multi-language support. Review console operation and handpiece controls during equipment onboarding.
Before treatment: Confirm the handpiece, patient assessment, selected parameters and documented protocol.
During operation: Follow the User Manual for aiming, positioning, foot-switch use and stopping the system.
Between sessions: Integrate cleaning, inspection, treatment records and service escalation into clinic procedures.
View full-size image↗ Workflow: Articulated delivery for positioning the handpiece around the treatment area.
Site review: Confirm movement and clearance; follow the manufacturer’s handling and inspection instructions.
View full-size image↗ Workflow: Physical controls for start, stop and access during the operating workflow.
Site review: Review controls during onboarding and confirm operator access in the planned room layout.
View full-size image↗ Workflow: Rear-panel access, electrical connection and ventilation planning for the selected model.
Site review: Request dimensions, weight and required clearances before arranging delivery or installation.
These categories support purchasing discussions, not treatment protocols or a claim that every use is authorized. Confirm device-specific indications, professional scope, patient selection, consent and aftercare before implementation.
Review focus: Resurfacing service fit, patient selection and expected recovery.
Before implementation: Confirm operator training, treatment endpoints and aftercare.
Review focus: Scar types considered for assessment and treatment planning.
Before implementation: Define assessment records, consent and follow-up requirements.
Review focus: Diagnosis, skin type and the proposed pigmentation concern.
Before implementation: Confirm the device-specific indication before offering the service.
Review focus: Texture concerns, pore appearance and realistic expectations.
Before implementation: Define treatment endpoints and post-procedure care.
Review focus: Suitability of resurfacing for the assessed skin-laxity concern.
Before implementation: Set realistic expectations; do not assume uniform tightening.
Review focus: Patient suitability and the planned response assessment.
Before implementation: Define treatment records, outcome review and follow-up.
Review focus: Appropriate diagnosis of the proposed benign lesion.
Before implementation: Confirm instructions, professional scope and facility approval.
Review focus: Written confirmation of the intended specialty indication.
Before implementation: Confirm authorization and training; probe availability is insufficient.
A practical reference for clinic owners, purchasing teams and qualified operators. Confirm model-specific specifications and commercial terms in the final written documents.
Regulator / database:
Health Canada · Medical Devices Active Licence Listing (MDALL).
Licence / classification:
No. 114258 · Class III · System.
Licence holder / manufacturer:
DioLaz Canada Inc.
First issue date:
2025-10-31.
Official licence name:
FRACTIONAL CO2 LASER THERAPY SYSTEM.
Status verification:
Check the live MDALL record for the current licence status before purchase.
The licence record identifies the licensed system; it should not be read as authorization for every application mentioned in marketing materials.
Laser / wavelength:
Fractional CO2 · 10,600 nm.
Output power:
Up to 40 W, adjustable.
Operating modes:
Fractional scanned mode; continuous-wave surgical mode.
Pulse duration:
0.4–4 ms, configurable.
Focal spot:
≤ 0.4 mm.
Scanner spot size:
0.1–2 mm, adjustable.
Beam delivery:
7-joint articulated arm.
Aiming beam:
650 nm red diode laser; < 5 mW.
Console interface:
12.1-inch colour touchscreen; programmable presets; multi-language support.
Cooling:
Air-cooled design.
System power:
1000 W.
Electrical supply:
110–240 V AC, 50/60 Hz.
Use these specifications for equipment comparison and purchase planning, not as treatment settings. Confirm the supplied model against the quotation, equipment label and current User Manual. Request dimensions, weight and installation clearances separately.
Confirm professional scope, insurance, equipment onboarding and access to current instructions.
Document patient assessment, consent, parameter selection, aftercare and incident escalation.
Confirm electrical service, access, ventilation, protective equipment and facility-specific safety arrangements.
Confirm cleaning and inspection schedules, maintenance responsibilities, service contacts and records.
View full-size image↗ Confirm the fractional scanner, focused handpiece and any specialty probe individually. List optional items separately from the included package.
Verify operator and patient eyewear, foot pedal, power cord and keys against the final packing list. The accessory photograph is for identification, not a guaranteed packing list.
Confirm the model and handpiece, itemized inclusions, delivery access, training scope, warranty and applicable program terms. Resolve any discrepancy before payment.
Final scope and terms must be consistent across the accepted quotation, invoice, agreement, packing list and applicable policies. Use the single Programs, Policies & Support directory near the top of this description.
If you have any questions, you are always welcome to contact us. We'll get back to you as soon as possible.
Shipping Information
At DioLaz Canada Inc., every order is handled with exceptional precision and care, ensuring your premium medical and aesthetic products reach you safely, securely, and promptly.
Customer Support
DioLaz Canada Inc. stands confidently behind the quality and reliability of our Medical and Aesthetic Devices. Our comprehensive warranty policy is carefully crafted to provide peace of mind to our valued customers.
Contact Us
customersupport@diolaz.com
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