Thermal and Chemical Disinfection Programme Capability
The G 7782 CD provides both validated thermal disinfection cycles and chemical disinfection programme options, extending reprocessing flexibility to temperature-sensitive instruments that cannot tolerate the temperatures required for thermal A0 disinfection. This dual capability makes it suitable for a wider range of clinical instrument types.
EN ISO 15883 Validated Thermal Disinfection
Thermal disinfection cycles are validated to EN ISO 15883, achieving defined A0 values that confirm effective microbial inactivation across instrument surfaces and lumens, providing the documented compliance evidence required in regulated healthcare settings.
Automated Multi-Phase Cycle
The unit sequences pre-wash, detergent wash, disinfection, and drying phases automatically, removing operator variability from the reprocessing workflow and ensuring consistent, repeatable outcomes across every cycle and user.
Full Cycle Data Logging for Audit Compliance
Every cycle generates a complete record of parameters and cycle status, supporting the audit trail and infection control documentation requirements of regulatory inspection and quality management frameworks.
Stainless Steel Construction
The 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 routine maintenance.
CE Certified and AMC-Ready
The G 7782 CD carries CE marking and meets EN ISO 15883 compliance requirements. Annual maintenance contracts are available from Medigear.uk to support ongoing cycle validation integrity and operational reliability.
