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Equipment Emitting Electromagnetic Waves 89/336/EEC Services
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EAAR MEMBER
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ISO 9001:2001 |
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EMC Marking and Labeling Workbook For Sale
Are you developing or selling a medical product that, 1) that has a new pre-market approval for the FDA; 2) is CE marked to the Medical Device Directive (93/42/EEC); or, 3) falls under the Canadian Medical Regulations (SOR/98-282)? If your product falls into any of these 3 categories, the 2nd Edition of IEC 60601-1-2:2001, Electromagnetic Compatibility Requirements and Tests for Medical Electrical Equipment is required as of November 1, 2004. This Workbook can help speed you along your way in complying with the marking and labeling changes to the standard.
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Design engineers, regulatory affairs personnel, or anyone who needs to understand the EMC marking and labeling requirements of IEC 60601-1-2:2001 2nd Edition, will find this Workbook an indispensable tool in developing EMC marking and labeling for their product, manuals and service manuals.
The Workbook provides the user with:
a classification tool;
a definition of which labeling and marking requirements apply;
sample wording for many of the labeling and marking requirements, warnings, etc., in the standard;
a tool for easy completion of appropriate tables from the standard; & Excel spreadsheets to perform calculations.
| Why spend thousands of dollars on internal and external resources figuring out these complex requirements for EMC marking and labeling when you can spend only $250.00 and cut your time and costs markedly. Your firm will spend less time and money creating EMC marking and labeling documentation. |
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