The availability and content of dental instrument manufacturers' decontamination information

British Dental Journal
E M RoebuckJ Walker

Abstract

The effective decontamination of reusable dental instruments is essential to reduce the risks from onward transmission of infectious diseases. There are therefore a number of legislative requirements placed upon manufacturers of medical devices (which includes dental instruments) to provide validated methods for the reprocessing of such devices. The aim of this study was to determine the availability and content of manufacturer's instructions for the reprocessing of reusable dental instruments. A database of reusable dental instruments with details of their manufacturers was collated from information received from three dental hospitals. A questionnaire was sent to all the manufacturers requesting information about the reprocessing instructions for their products. The response from each manufacturer was assessed for the quality of the information and compliance with the British, European and International Standard, BS EN ISO 17664 (2004). The database from the three dental hospitals included over 800 items supplied by 54 different manufacturers/suppliers. Forty protocols were available for assessing compliance with BS EN ISO 17664 (2004). These protocols accounted for 25 (46%) manufacturers covering 300 devices. The majority (9...Continue Reading

References

Feb 5, 2000·The Journal of Hospital Infection·W A Rutala, D J Weber
Jul 30, 2002·The Journal of Hospital Infection·A SmithJ Bagg
Sep 12, 2002·Primary Dental Care : Journal of the Faculty of General Dental Practitioners (UK)·Christine L Whitworth
Apr 7, 2004·The Journal of Hospital Infection·B ZühlsdorfH Martiny

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Citations

May 14, 2016·British Dental Journal·D SonntagW H M Raab

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