Quick Overview

At GT2 Healthcare, we combine cutting-edge technology and industry best practices to offer:

• ETO Sterilisation Services for heat - or moisture-sensitive devices
• Product Validation at our on-site laboratory
• Bioburden Testing to meet regulatory standards
• Certification & Reporting for compliance
• Training & Qualification Programmes accredited by government bodies

We are building something extraordinary and would love for you to be part of it. Stay tuned for exciting developments and progress photos of our facility.

Together, let’s shape a safer and healthier future for medical devices.

+603 7732 6886
info@gt2healthcare.com

+603 7732 6886

info@gt2healthcare.com

Mon - Fri 9:00 - 17:30. Closed on Sat, Sun & Public Holidays

Technology

Precision Sterilisation. Proven Safety.

Why ETO Sterilisation?

The Power of Ethylene Oxide (ETO) Sterilisation

Ethylene Oxide (ETO) sterilisation is a low-temperature process that uses a specialised gas to eliminate a wide range of microorganisms, including bacteria, viruses, and fungi. Unlike heat-based methods that can compromise delicate materials, ETO effectively penetrates complex device geometries, porous materials, and sealed packaging without causing damage. This makes it particularly advantageous for sterilising heat- or moisture-sensitive medical devices, such as catheters, sutures, and certain plastics or electronics.

 

As a result, ETO has become a trusted method in the healthcare industry—offering flexibility, preserving product integrity, and ensuring patient safety. Additionally, ETO’s proven reliability and gentle treatment approach stand in contrast to methods like steam or radiation sterilisation, which may alter product properties. With ETO, manufacturers gain confidence in both the efficacy of the sterilisation process and the quality of their finished products.

Compliance & Global Standards

At GT2 Healthcare, we adhere to the strictest international regulatory frameworks, ensuring that every sterilisation cycle meets global safety and quality benchmarks.

✔ Validated ETO sterilisation processes
✔ Medical device quality management systems
✔ Regulatory Audits – Continuous internal and external evaluations to maintain excellence

By upholding these rigorous standards, we minimise risk, enhance product reliability, and provide manufacturers with confidence in our processes.

Sustainability & Environmental Responsibility

While ensuring the highest standards in sterilisation, GT2 Healthcare is committed to environmental stewardship. Our sustainability initiatives include: We believe that effective sterilisation should protect both human health and the planet. By continually refining our protocols and investing in green technologies, we are shaping a future where sterilisation excellence goes hand in hand with environmental responsibility.

Energy-Efficient Sterilisation Chambers

Reducing power consumption without compromising performance

Optimised Aeration Systems

Minimising residual emissions for safer environmental impact

Eco-Friendly Research & Development

Exploring innovative sterilisation solutions that balance safety with sustainability

Processes

At GT2 Healthcare, we adhere to a meticulous, step-by-step sterilisation process to ensure the highest standards of safety and quality for your products. Our end-to-end process guarantees not only effective sterilisation but also the safety and integrity of your products, providing peace of mind for manufacturers and end-users alike.

Receiving & Inspection

Upon arrival, goods from the manufacturer are carefully checked against delivery notes and purchase orders. Each batch is inspected for proper packaging, labelling, and any visible damage before being accepted for sterilisation.

Preconditioning

Products are placed in a controlled environment where temperature and humidity are carefully managed. This preconditioning step ensures that the items reach the required internal moisture and temperature levels for optimal ETO penetration during sterilisation.

ETO Sterilisation Cycle

Once properly conditioned, the products are loaded into a sterilisation chamber, which is then sealed and filled with a precise concentration of ETO gas. Temperature, humidity, and exposure time are tightly controlled to ensure thorough microbial inactivation. The chamber’s conditions are continuously monitored to maintain strict compliance with validated parameters.

Aeration (Degassing)

After the sterilisation cycle, products are moved to an aeration area where they are allowed to off-gas any residual ETO. This stage ensures that the finished goods meet safety thresholds for residual chemicals, preserving product integrity and making them safe for end-users.

Quality Checks & Documentation

Biological indicators, chemical indicators, and other validation measures are reviewed to confirm the effectiveness of the sterilisation cycle. Comprehensive records are kept, and accreditation reports are prepared to maintain a clear audit trail and guarantee regulatory compliance.

Final Packaging & Dispatch

Once all quality checks are complete, the sterilised products are securely packaged and prepared for shipment. Logistics arrangements are made according to the client’s requirements, ensuring timely and efficient delivery of sterilised goods back to the client’s destination.