DioLaz Health Canada Licensed Picosecond Laser for Tattoo Removal & Skin Rejuvenation
$67,800.00 CAD
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DioLaz Health Canada Licensed Picosecond Laser for Tattoo Removal & Skin Rejuvenation
$67,800.00 CAD
Product details
Description
Health Canada Licensed • MDL 115451
Health Canada Licensed Picosecond Laser for Professional Clinics
Dual-wavelength 1064 / 532 nm performance with 450 ps pulse delivery, adjustable energy, up to 10 Hz repetition and 2–10 mm spot control for professional tattoo-removal, benign-pigment and skin-rejuvenation workflows.
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Health Canada Licensed
Verify Licence →Class III Medical Device • MDL 115451 • Licence Holder (Manufacturer): DioLaz Canada Inc.
System Performance
Picosecond Control for Professional Treatment Planning
The platform combines ultra-short pulse delivery with adjustable energy, repetition-rate and spot-size control for clinic workflows that require precision and repeatability.
01Pulse Duration450 ps
02Pulse Energy1064 nm: 20–500 mJ • 532 nm: 10–250 mJ
03Repetition Rate1–10 Hz
04Spot Size2–10 mm continuous zoom
Treatment Technology
Dual-Wavelength Treatment Planning
Wavelength selection supports differentiated pigment targeting across professional tattoo-removal and pigment-treatment workflows.
Supports treatment planning for darker tattoo inks and deeper pigment, with lower melanin absorption than 532 nm.
Supports selected superficial pigment and warm-toned tattoo inks such as red, orange and yellow.
Final wavelength, energy, spot size, repetition rate and treatment endpoints must follow professional training, client assessment, applicable scope of practice and the current DioLaz User Manual.
Clinical Application Portfolio
One Platform, Multiple Professional Service Lines
Application selection depends on operator qualifications, client assessment, indication, skin type and the approved treatment workflow.
Tattoo Removal
Professional and amateur tattoo workflows with wavelength selection based on ink colour, depth and client assessment.
Benign Pigmented Lesions
Selected epidermal and dermal pigment concerns assessed and treated by qualified professionals using appropriate parameters.
Skin Rejuvenation
Non-ablative picosecond workflows intended to support texture, pore and overall skin-quality treatment plans.
Clinical Design
Beam Delivery, Treatment Interfaces & System Access
Articulated Arm
Beam delivery with stated ≥95% transmission efficiency.
Interchangeable Handpieces
Two treatment interfaces: one standard handpiece and one focus-lens handpiece.
Rear Connections & Ventilation
Power, ventilation and service-access areas for installation and maintenance planning.
Procurement Reference
Technical, Regulatory & Implementation Information
Structured for clinic owners, procurement teams and qualified operators reviewing regulatory status, system capability, clinical workflow, site readiness and order scope.
Review PurposePre-Purchase Due Diligence
Canadian LicenceClass III • MDL 115451
Laser Platform1064 / 532 nm • 450 ps
Physical Profile130 kg • 100 × 42 × 98 cm
Document hierarchy: final configuration, supplied accessories, training, warranty, delivery and commercial terms are governed by the issued quotation, invoice, signed agreement and applicable DioLaz policies.
01 Regulatory & Supplier Record
Field
Record
Regulator
Health Canada
Database
Medical Devices Active Licence Listing (MDALL)
Licence Status
Active
Device Class
Class III Medical Device
Medical Device Licence
MDL 115451
Licence Type
Device Family
Licence Name
PICOSECOND LASER SYSTEM
Licence Holder / Manufacturer
DioLaz Canada Inc.
First Issue Date
2026-05-25
02 System Performance Envelope
Specification
Value
Laser Type
Picosecond Nd:YAG laser system
Wavelengths
1064 nm & 532 nm
Pulse Energy
1064 nm: 20–500 mJ; 532 nm: 10–250 mJ (adjustable)
Pulse Duration
Approximately 450 ps
Repetition Rate
1–10 Hz (adjustable)
Spot Size
2–10 mm continuous zoom
Beam Delivery
Articulated arm with stated ≥95% transmission efficiency
Aiming Beam
650 nm red diode laser pointer
Cooling System
Internal air and closed-loop water cooling
Included Handpieces
Two interchangeable handpieces: standard and focus lens
Power Supply
2500 W; 110 V AC; 50/60 Hz
Dimensions
100 × 42 × 98 cm (W × D × H)
Net Weight
130 kg
Reference specifications support product comparison. Final operating parameters must follow client assessment, professional training, applicable scope of practice and the current DioLaz User Manual.
03 Clinical Workflow & Practice Fit
Tattoo-Removal Workflow
Dual-wavelength delivery supports colour- and depth-based treatment planning. Session count, energy, overlap and endpoints remain case specific.
Pigment Workflow
Selected benign pigmented lesions require appropriate assessment, indication confirmation and parameter selection by a qualified operator.
Rejuvenation Workflow
Non-ablative picosecond applications can complement clinic skin-quality and texture programs when supported by training and protocol.
Clinic Integration
The platform can support dermatology, medical-aesthetic and tattoo-removal service lines within one professional device workflow.
Implementation controls
- Qualified operators should complete applicable product training and review the current User Manual before clinical use.
- Client assessment, contraindication screening, consent, selected parameters and treatment endpoints should be documented.
- Wavelength, energy, repetition rate, spot size, overlap and pass count must be selected for the individual indication and client.
- Commercial planning should use local pricing, expected utilization, staffing, maintenance, financing and the issued quotation; no revenue result is guaranteed.
04 Safety, Site Readiness & Scope of Supply
Core System & Beam Delivery
Mobile Picosecond Laser console with articulated-arm beam delivery and professional operating controls.
Treatment Interfaces
Two interchangeable handpieces are listed: one standard handpiece and one focus-lens handpiece.
Electrical & Physical Profile
2500 W; 110 V AC; 50/60 Hz; 100 × 42 × 98 cm; 130 kg net weight.
Site Readiness Review
Confirm delivery access, floor level, doorway or elevator clearance, electrical service, treatment-room readiness and local laser-safety controls before order approval.
Scope of supply and order documents
Final included accessories, crate and freight scope, installation, training, warranty, service and commercial terms must match the issued quotation, invoice, signed agreement and current DioLaz policies. Marketing images should not be used to infer unlisted accessories or services.
Need product, configuration or purchasing guidance?
Discuss clinic fit, documentation, demonstration and ordering with a DioLaz Product Specialist. Sales email for procurement records: Sales@diolaz.com
For professional use only. Contraindications, precautions, client selection and treatment parameters must be reviewed in the current DioLaz User Manual before clinical use.
If you have any questions, you are always welcome to contact us. We'll get back to you as soon as possible.
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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.
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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.
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Contact Us
customersupport@diolaz.com
