ISO /(R) Medical devices—Symbols to be used with medical device labels, labeling, and information to be supplied—. Part 2: Symbol. ANSI/AAMI/ISO /(R) Medical devices – Symbols to be used with medical device labels, labeling and information to be supplied – Part 2. Find the most up-to-date version of ISO at Engineering
|Published (Last):||6 June 2012|
|PDF File Size:||1.8 Mb|
|ePub File Size:||14.25 Mb|
|Price:||Free* [*Free Regsitration Required]|
This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3.
The ISO series of standards addresses symbols that can be used to convey information that is essential for the safe and proper use of medical devices. Learn more about the cookies we use and how to change your settings. ISO proposes solutions to these problems through the use of internationally recognized symbols, with precisely defined meanings, that are independent of language.
Your basket is empty. When the processes detailed in this part of ISO have been carried out, the probability of misinterpretation of symbols accepted in ISO is reduced. Symbol development, selection and validation. In addition, some users and regulatory authorities have concerns that the unrestricted use of symbols without validation can represent a hazard. However, the proliferation of symbols without control and harmonization is undesirable and detracts from the effectiveness of using symbols to convey information for safety.
The information can be required to be presented on the device itself, as part of the label or provided with the device. The use of standardized symbols agreed by consensus on an international basis can address the confusion that users can experience when presented with labelling in a number of different languages.
Many countries require that their own language be used to present textual information with medical devices. Establishing need Providing guidance on development of symbols Carrying out testing to make sure that the candidate symbol is suitable for adoption and use.
As such, in most regulatory domains the symbols are required to be presented with the device. You may find similar items within these categories by selecting from the choices below:.
Symbol development, selection and validation The ISO series of standards addresses symbols that can be used to convey information that is essential for the safe and proper use of medical devices. Symbols to be used with medical device labels, labelling, and information to be supplied.
Symbol development, selection izo validation BS ISO specifies a process for developing, selecting and validating symbols for inclusion in ISO This part of ISO includes methods for validating those candidate symbols being proposed for inclusion in ISO Worldwide Standards We can source any standard from anywhere in the world. Good clinical practice BS EN BS ISO is not restricted to symbols intended to meet regulatory requirements or specified in regulatory guidelines on labelling.
As with any risk control measure, the manufacturer needs to verify the effectiveness of the information for safety before it can be accepted. This standard is in two partsunder the general title Medical devices – Symbols to be used with medical device labels, labelling and information to be supplied: Bei Aufschriften von Medizinprodukten zu verwendende Symbole, Kennzeichnung und zu liefernde Informationen.
You may experience issues viewing this site in Internet Explorer 9, 10 or Click to learn more. Symbol development, selection and validation Status: Much of the information required on a medical device itself, as part of the label, or provided with the device constitutes information for safety within an integrated approach to risk management.
Take the smart route to manage medical device compliance. This presents problems to device manufacturers and users. Search all products by.
BS ISO 15223-2:2010
Entwicklung von Symbolen, Auswahl und Bewertung. If the symbol validation process detailed in BS ISO has been complied with, then the residual risks associated with the usability of a medical device symbol are presumed to be acceptable unless there is objective evidence to the contrary.