VALIDATION SERVICES

The H.S.E Code of Practice recommends that endoscope reprocessors must be validated periodically to ensure that endoscopes are cleaned properly, and that they are sterile immediately after being washed.

EN 15883 and HTM 2030 are the guidelines for the validation of the endoscope reprocessors, and specify all of the tests which should be carried out. These tests depend upon the make and model of machine. Medipure Ireland can provide validations for most manufacturers of endoscope reprocessors, including Wassenburg, Labcaire, Lancer and Steris.

We also specialise in validation of various models of drying storage endoscope cabinets, offering devices to check both functionality and performance to make sure that the cabinet keeps the endoscopes in optimal sterile conditions before their use in patients.

Medipure Ireland Ltd also provides a Cleanroom monitoring service. Cleanrooms, Changing rooms, Manufacturing areas and Theatres can now use our services.

As a Microbiological Validations Company, Medipure Ireland do all microbiological testing at our Dublin based lab, all of which is tested by fully trained Microbiologists. With eight years experience that Medipure (UK) Ltd has in the validation of endoscope reprocessors, we have expert knowledge and expertise, and aim to offer the best service possible, as well as advice on best practice.