Precision therapy for targeted results in just 10 minutes daily
Your Dedicated Redlight (NIR) Therapy Panel Supplier
Redlight Therapy Beds
When sourcing your Redlight Therapy Panels, for Salon or home use, precision, reliability, and innovation are non-negotiable. We stand as your dedicated partner, delivering superior quality panels designed for performance and market success. Please note, all our systems are ISO 13485 MDsap Certified for total peace of mind.
We offer a full range of beds or a bespoke service offering 7 wavelengths, from 480nm-630nm-660nm-810nm-830nm-850nm-1060nm. Please (NIR) facemasks, belts,
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What if we said...
“If there were a pill that was proven to have powerful anti-ageing effects on our skin, combat our neurological diseases, fight depression and anxiety, increase fat loss, speed recovery, increase strength and endurance, combat certain autoimmune conditions and speed healing from injury, all with little to no side effects; It would be a Billion Dollar Drug...
...That drug exists but it’s not a pill, it’s near infrared light therapy”
Professor Michael Hamblin, Harvard Med School
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ISO 13485 is a quality management system
ISO 13485 is a quality management system (QMS) standard specifically for the medical device industry, ensuring organizations consistently produce medical devices and related services that meet both customer and regulatory requirements. It provides a framework for managing quality throughout the entire lifecycle of a medical device, from design and manufacturing to installation and servicing, with a primary focus on patient safety.
Key aspects of ISO 13485
- Focus on safety and regulation: The standard emphasizes patient safety and helps organizations comply with the complex regulations of the medical device sector.
- Lifecycle management: It applies to all stages of a medical device's life, including design, development, production, storage, distribution, installation, servicing, and disposal.
- Process-based approach: Based on the ISO 9000 series, it uses a process-based approach to ensure quality and encourages continuous improvement based on objective data.
- Market access: Achieving ISO 13485 certification is often a requirement for market access in many international regions and is a key component of programs like the Medical Device Single Audit Program (MDSAP).
- Who it applies to: The standard is applicable to any organization involved in the medical device sector, from manufacturers to suppliers.
Benefits of ISO 13485
- Ensures consistent quality: Helps organizations maintain a consistently high level of quality for their products and services.
- Promotes patient safety: By implementing rigorous quality controls, it directly contributes to the safety of patients using medical devices.
- Facilitates global market access: Certification demonstrates compliance with international standards, which is crucial for exporting medical devices.
- Increases efficiency: A well-implemented QMS based on the standard can lead to more efficient processes and better risk management.
- Improves credibility: Certification is a valuable credential that builds trust with customers, regulators, and other stakeholders.