European EN and International ISO standards Essay

The abbreviations EN refers to European Norm while ISO refer to International Standards Organization. Endoscopy literally way looking inside and it is ordinarily refers to look inside the body usually in relation to medical reasons using an instrument called an endoscope. It is employd to reckon the interior parts of a hollow organ or fossa of the body, and they argon inserted directly into the organ.The endoscopes, especially flexible endoscopes atomic number 18 usually confused but can be reused but require very eccentric conditions for reuse in respect to their decontamination. It is not only their outer surfaces that atomic number 18 exposed, but as well as their air channels, water channels and even their accessories that modify them to function in the right manner. Their exposure to body fluids and other contaminants substance that their reuse has to be very carefully looked into so as to repress spread of diseases. It is as well as important to realize that most e ndoscopes are disturb labile and cannot be autoclaved meaning they change under different oestrus conditions.European (EN) and International (ISO) standards that would be applicable to an endoscope decontamination unit (EDU) in the UKAs abstracted from EN ISO 15883, information from the manufacturers should be given prior to purchasing the endoscope. This implies that the manufacturer provides information such the best disinfectants to use with that fussy endoscope and what is judge when cleaning, for example the bacteria expected to be found there and also if the disinfectant in question is compatible with the automatic reprocessor in which it is universe used. (Gurusamy Manivannan, 2008)As per BS EN ISO 15883-1, a temperature recorder having no less than ten sensors should be used, and the specifications are well indicated in the ISO standard. This is because the endoscopes are commove labile, and temperature may affect the chemical compositions of the accessories or other chemicals involved.The manufacturer should also establish the worst conditions under of the devices configuration. Such conditions encompass temperature, detergent dousing and surrogate device configuration. This also includes water flow pressure for use during testing. This may also be categorized in a mistakable manner as biocompatibility testing where limits such as residual limits are stipulated as per ISO 10993. (Denise Sheard, 20120The calibrations should be checked in accordance with ISO 10012-1 for uniformity purposes. These are usually dictated by manufacturers using a validated order of applying a sensible reference. Each instrument should also be designate with a unique reference number. This is important when measuring passage of fluids or drugs so as to get accurate and true results.The standard prEN ISO 15883-1-2004 has a clause that indicates that the manufacture shall all addition information associated with the use and decontamination of the particular endoscop e. Information such as maximum flow and pressure of fluids indoors each channel in the device and the maximum possible permissible restriction of flow within each channel is deemed important and moldiness be provided. (James Walker, 2014)There is also a standard similar to twain that the manufacturers may be requested to give information concerning the device at any stage, and act as consultants. This is stipulated in prEN ISO 15883-1-2004. This is important when complications arise that personnel department involved were not expectingReferencesGurusamy Manivannan, Disinfection and decontamination principles, applications and related issues. Boca Raton CRC Press/Taylor & Francis Group, 2008Denise Sheard , A practical channel to decontamination in healthcare . Hoboken John Wiley & Sons, 2012.James Walker, Decontamination in hospitals and healthcare. Oxford Woodhead Publishing, 2014Source register