Every Intermed product is a testament to our mandate: absolute sterile barrier integrity. From raw material to final dispatch, our protocol ensures uncompromised protection across all healthcare consumable lines.
Our 4-Stage Verification Protocol
Raw Polymer Inspection
Particle Filtration Testing
Gamma Sterilization
Lot Batch Traceability
Incoming medical-grade polymers undergo precise spectroscopic analysis and material stress testing to ensure foundational integrity.
Advanced cleanroom air filtration systems and product surface particulate counts are continuously monitored to guarantee a sterile environment.
Post-packaging, products are subjected to validated gamma sterilization cycles, ensuring complete pathogen inactivation and barrier safety.
Each production lot is meticulously logged and tracked, providing full traceability from manufacturing line to end-user facility.
Verified Regulatory Credentials
ISO 13485 Certified
CE Directive 93/42/EEC
WHO-GMP Audit Clearance
Our quality management system meets international standards for medical device manufacturing, ensuring consistent product excellence.
All products comply with European Union health, safety, and environmental protection standards, enabling seamless market access.
Regularly audited against World Health Organization Good Manufacturing Practices, affirming our commitment to global pharmaceutical quality.