Posted In: Blog , Blog Morulaa Biocompatibility is a measurement of how compatible a device is with a biological system not generating any local or systemic responses from a living system or tissue. In the simplest sense, a biocompatible material or device does not harm the patient. From a regulatory view, it is a series of tests that are used to determine the toxicity resulting from contact of the parts of medical devices or combination products with the body. A medical device may consist of materials that are biocompatible, although the device itself requires biocompatibility testing and all testing is performed on the final product.
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Shaktizahn Activation of your subscription failed — please try again later or contact us. Part 18 was substantially revised and is now proposed to be converted from a Technical Specification to a full standard. It does not apply to tests performed on invertebrate animals and other lower forms; nor other than with respect to provisions relating to species, source, health status, and care and accommodation does it apply to testing performed on isolated tissues and organs taken from vertebrate animals that have been euthanised.
Continue shopping Proceed to checkout. The concept may also be applied more generally to unidentified contaminants. Animal assays will be with us for a while yet — but TC is making real progress on non-animal alternatives. ISO does not deal well with biological evaluation of respiratory devices — such as ventilators, masks and inhalers — which have indirect patient contact via the gas pathway. The outcome was to allow an extension of exemptions for haemodialysis to cover peritoneal dialysis and other blood purifiers.
Animal welfare requirements Status: Animals, Animal welfare, Planning, Personnel, Laboratory techniques, Test specimens, Laboratory workers, Laboratory testing, Medical equipment, Surgery, Biological analysis and testing, Laboratory animals, Testing conditions. Username or password invalid. It is not possible to buy in the shop — please contact us. You may experience issues viewing this site in Internet Explorer 9, 10 or Search all products by. Accept and continue Learn more about the cookies we use and how to change your settings.
The outcome was addition of MEM elution test to the Annex of the revision draft. May 9, You may find similar items within these categories by selecting from the choices below:.
The concept is straightforward — if it can be shown that an impurity is below the TTC, then it is assumed that the level of contamination is of no significant risk and no further evaluation is required regard to that impurity. This should provide a safety assessment approach based on assessment against acceptable limits of volatile organics and particulates which is not only cheaper and simpler to perform — but also much more robust and protective of the patient.
An iwo on risk management. Take the smart route to manage medical device compliance. You must be logged in to sign up for monitoring You must be iwo in to sign up for subscription. Worldwide Standards We can source any standard from anywhere in the world. Kontakt venligst Dansk Standard. Your basket is empty. We can help you with developing your evaluation strategy, dealing with test laboratories and preparation of expert reports. Click to learn more. Learn more about the cookies we use and how to change your settings.
Are you ixo you want to unsubscribe? Nanomaterials, EO residues, hemolysis and more. December Biological evaluation of medical devices Framework for identification and quantification of potential degradation products. Please choose number of devices you want to open the document on. New content on postmarket monitoring and electronic records. Biological evaluation of medical devices — Part 2: Work is also underway on a new Annex on complement testing possible in vitro thrombogenicity models to replace the current canine model.
It applies to tests performed on living vertebrate animals, other than man, to establish the biocompatibility of materials or medical devices. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. Activation of monitoring failed — please try again or contact us. TOP Related Posts.
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Tygozahn The concept is straightforward — if it can be shown that an impurity is below the TTC, then it is assumed that the level of contamination is of no significant risk and no further evaluation is required with regard to that impurity. The concept may also be applied more generally to unidentified contaminants. ISO — Wikipedia Animal welfare requirements Status: The outcome was to allow an extension of exemptions for haemodialysis to cover peritoneal dialysis and other blood purifiers. An annex on risk management. Kontakt venligst Dansk Standard. Please download Chrome or Firefox or view our browser tips. Separately work is underway to introduce non animal based test methods for genotoxicity, irritation and sensitization.
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