EN ISO 15883 Validated Thermal Disinfection
The G 7825 delivers thermal disinfection cycles validated to EN ISO 15883, achieving defined A0 values that confirm effective microbial inactivation across instrument surfaces and lumens. This validation provides the documented evidence required by infection prevention standards and decontamination compliance frameworks in regulated clinical environments.
Automated Multi-Phase Wash and Disinfection Cycle
The unit sequences pre-wash, detergent wash, thermal disinfection, and drying phases automatically without manual intervention, removing operator variability from the reprocessing workflow and ensuring consistent, repeatable disinfection outcomes across every cycle and operator.
Full Cycle Data Logging for Audit Compliance
Every cycle generates a complete record of temperature profiles, time parameters, and cycle status, supporting the documentation requirements of infection control quality management and regulatory inspection. This audit trail supports CQC and equivalent inspection compliance across all clinical settings.
Stainless Steel Construction for Long-Term Reliability
The internal wash chamber and instrument contact surfaces are fabricated from professional-grade stainless steel, engineered to withstand sustained thermal and chemical exposure for long service life and straightforward routine maintenance.
CE Certified and EN ISO 15883 Compliant
The G 7825 carries CE marking and meets EN ISO 15883 requirements, satisfying procurement compliance for regulated healthcare settings. Full certification and validation documentation is available from Medigear.uk.
AMC-Ready Design for Ongoing Service Support
The G 7825 is designed to support scheduled preventive maintenance through annual maintenance contracts available from Medigear.uk, ensuring continuous cycle validation integrity and operational reliability throughout its clinical service life.
