CE ISO Certified 1600-2400W Diode Laser Hair Removal Device

Name: CE ISO Certified 1600-2400W Diode Laser Hair Removal Device
Brand: Beijing Winkonlaser Technology Limited
SKU: 1968063662

Beijing, ChinaBeijing Winkonlaser Technology Limited

US$1,150.00-5,500.00

1 Piece

Sample price:US$5500.00/piece.Request sample

Product profile

Customization

Available

Type

Laser Beauty Equipment

Theory

Laser

Model NO.

DL1500

Application

Salon

Portable

Non Portable

Laser Type

808nm Diode Laser

Wavelength

808nm+755nm+1064nm

Laser Power

800W/1000W/1200W/1600W

Spot Size

14*25mm+12*40mm

Function

Permanent Hair Removal

Keyword

Laser Hair Remvoal

Warranty

3 Years

Transport Package

Air Case

Specification

70*75*120

Trademark

winkonlaser

Origin

China

Production Capacity

500

Company profile

Years of Export ExperienceR&D CapabilitiesFast DeliveryQuality Assurance

Beijing Winkonlaser Technology Limited

Beijing, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 11 years CertifiedNearest Port: Beijing PortAverage Response Time: ≤1.73h

AI-Powered supplier vetting

SummaryWinkonlaser is an instrument and medical-device supplier with sales, engineering, and service teams. It reports OEM service for well-known brands, ODM capability, recent new-product development, and broad customization services. Manufacturing information indicates two production lines, 31–40 quality-control staff, and stated output of 2,500 pieces for several laser and aesthetic-equipment categories. Export activity represents 90% of total sales and has continued for 11 years. However, the supplier lacks an available SDK, does not continuously reconcile production quantities by batch, and has no documented standard operating procedure for outsourced manufacturing. Finished products are checked by packing staff, while service procedures are mixed: complaint handling and corrective/preventive actions have documented procedures and records, but the overall service-capability assessment procedure does not. Certification, customer case details, and environmental and fire-drill status are not sufficiently...

Supplier typeThe stated business scope covers instrument sales, electronic products, Category I and II medical devices, licensed Category III medical-device business, and import/export agency activities. This identifies the supplier as an instrument and medical-device business, although the provided information does not establish a narrower manufacturer classification.

After-Sales capabilityWinkonlaser reports a dedicated service team and customer-service focus. It has clear procedures and followed records for corrective and preventive actions and customer complaints, but lacks a written procedure or followed records for the overall effective supplier service-capability assessment.

R&D capabilityThe supplier reports new products during the past year, ODM services, and multiple customization-based design services. It explicitly has no available SDK, which limits the evidenced level of software-development or integration support, but does not negate the stated product R&D capability.

Production capacityThe supplier operates two production lines, reports 31–40 quality-control staff, and lists 2,500 pieces of annual output across several laser and aesthetic-equipment categories. Nevertheless, it does not continuously reconcile quantities by batch and has no standard operating procedure for outsourced manufacturing, indicating documented production-control gaps.

Customization capabilityThe supplier explicitly offers customization from samples and designs, full, minor, and flexible customization, supported by ODM availability. These statements directly evidence broad customization capability.

Client casesThe supplier states that it provides OEM services for well-known brands, which is evidence of brand-related OEM experience. No brand names, project descriptions, references, or verifiable case details are supplied, so the depth of customer-case experience cannot be fully assessed.