Steris Blog

Effective sterile barrier packaging, including validated blister systems, is essential to maintain medical device sterility. Many failures occur due to packaging errors, not sterilisation. Steris Surgical Solutions supports manufacturers with packaging validation, ETO compatibility trials and compliance to ISO 11607, ensuring safe, audit-ready products.

India’s first end-to-end ETO sterilization solution for medical devices. We handle every step—from precision mold creation to advanced sterile packaging using Tyvek, followed by validated sterilization cycles and audit-ready documentation. Our integrated process ensures complete sterility, safety, traceability, and compliance, providing manufacturers with a reliable, high-quality solution all under one roof.

Surgical instruments are the frontline tools in life-saving procedures, and their sterility is non-negotiable. At Steris Surgical Solutions, we ensure that every scalpel, forceps, retractor, and clamp is sterilized using a precisely validated Ethylene Oxide (EtO) process—ideal for preserving the sharpness, structure, and function of delicate surgical tools. Our EtO sterilization provides: ISO 11135-compliant protocols with biological indicator validation Packaging in Tyvek se

Steris Surgical Solutions provides ETO sterilization services, ensuring pharma APIs meet global safety standards for safe manufacturing.

From spice shelves to export woes, India tackles Ethylene Oxide contamination head-on. FSSAI leads the charge for food safety. #SpiceScandal

Steris Surgical Solutions ensures surgical safety in India with advanced EtO sterilization services, expertise, and commitment to quality.