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"Biocompatibility Protocols for Medical Devices and Materials provides comprehensive coverage of the basic science and toxicological testing protocols necessary for the risk assessment and safety analysis of medical devices and materials which are based on the ISO guidelines for body contact and duration of contact. The book begins with device/component selection for toxicological experiments and provides an introduction to topics such as sensitization, irritation tests, material-mediated pyrogenicity, and bacterial-mediated pyrogenicity. Toxicology-related chapters explain the protocols for cytotoxicity, acute systemic toxicity, repeated-exposure systemic toxicity, genotoxicity, carcinogenicity, and reproductive toxicity testing. Biocompatibility Protocols for Medical Devices and Materials is a practical guide that provides step-by-step toxicological protocols ranging from materials selection to data interpretation for toxicologists, biomedical researchers, healthcare professionals, product developers, and others working in risk assessment and safety analysis of medical devices"--
Biocompatible Materials. --- Materials Testing. --- Testing, Hemocompatible Materials --- Biocompatibility Testing --- Biocompatible Materials Testing --- Hemocompatibility Testing --- Testing, Biocompatible Materials --- Hemocompatibility Testings --- Hemocompatible Materials Testing --- Materials Testing, Biocompatible --- Materials Testing, Hemocompatible --- Testing, Biocompatibility --- Testing, Hemocompatibility --- Testing, Materials --- Testings, Biocompatibility --- Flexural Strength --- Biocompatible Materials --- Bioartificial Materials --- Hemocompatible Materials --- Biomaterials --- Bioartificial Material --- Biocompatible Material --- Biomaterial --- Hemocompatible Material --- Material, Bioartificial --- Material, Biocompatible --- Material, Hemocompatible --- Materials Testing --- Biomimetic Materials --- Regenerative Medicine --- Medical instruments and apparatus --- Biomedical materials. --- Toxicity testing. --- Equipment and Supplies --- Testing.
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This comprehensive resource features in-depth discussions of important guidelines and regulations you will need to understand and properly meet medical device code-related requirements. Focusing on the practical application of the regulations, the Medical Device Guidelines and Regulations Handbook delivers clear explanations, real-world examples, and annotation on the applicable provisions that will allow you to safely and confidently choose materials and processes for medical device development, testing, and manufacturing. A critical resource for researchers and professionals in the medical device field; Thoroughly covers ISO 10993, ISO 22442, ISO 14971, ISO 13485, ISO 21534, REACH, RoHS, CLP, EU MDR; Presents simplified guidelines and regulation points.
Human biochemistry --- Biotechnology --- medische biochemie --- bio-engineering --- biotechnologie
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Medical instruments and apparatus --- Biomedical engineering. --- Safety regulations. --- Clinical engineering --- Medical engineering --- Bioengineering --- Biophysics --- Engineering --- Medicine
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