Medical Laser Equipment Testing

CTNT Zhongwei Testing provides medical laser product testing and certification services for you! Including but not limited to: laser surgical equipment, laser therapy equipment, laser diagnostic instruments, low‑level laser external therapy devices, and other medical laser products.

I. Service Overview

As a professional organization specialized in laser equipment testing and certification, CTNT Zhongwei Testing has long been committed to providing one‑stop medical laser equipment testing and certification services for medical laser equipment manufacturers, producers, agents, distributors, as well as universities, colleges and research institutions.

Our services cover a full range of medical laser equipment, including but not limited to: laser surgical equipment, laser therapy equipment, laser diagnostic instruments, low‑level laser external therapy devices, etc.

II. Service Scope

Our testing services are available to global customers, covering various types of medical lasers, such as solid‑state lasers, gas lasers, semiconductor lasers, liquid lasers, fiber lasers, etc.

III. Testing Standards

IEC 60825-1, EN 60825-1, 21 CFR 1040.10, GB 7247.1, etc.

IV. Testing Items

Laser (eye) safety classification certification, laser performance parameter testing (wavelength, power, spectral width, etc.)

V. Service Advantages

• More than 70 laser‑related authorized standards

• Over 120 laser testing capability parameters

• Power measurement range: pW to 5 kW

• Pulse measurement down to ps level

• Comprehensive coverage of laser safety and performance measurement capabilities and authorizations

• Testing capabilities and experience covering: consumer lasers, aesthetic lasers, measurement lasers, industrial lasers, medical lasers, military lasers, etc.

• All testing instruments and equipment are imported to ensure testing accuracy

VI. Solutions

1. Laser class testing and assessment for laser modules, laser assemblies, and finished laser products

2. Laser product label inspection and guidance on proper label creation

3. Structural and design guidance for laser products (including protective barriers, attenuation, interlocks, user instructions, etc.)

4. Laser beam quality analysis

5. Test reports for laser products or lasers (including IEC 60825, 21 CFR 1040.10, quality inspection reports, etc.)

6. Laser FDA registration and certification (including initial report, obtaining accession number, guidance on filling out Form 2811 for export, annual reports, registration documentation collection and guidance, etc.)

7. Technical consulting on special requirements for laser application scenarios and products (including industrial processing, aesthetics, medical, pointing devices, stage lighting, toys, etc.)

8. Information and case studies on cutting‑edge laser technology developments

VII. Service Process

1. Consultation and communication

2. Testing application submission

3. Sample mailing

4. Testing execution

5. Report delivery