Electro-Magnetic Compatibility Testing of Medical DevicesGet your FREE Guide to Electromagnetic Compatibility
Electromagnetic compatibility is an important and integral part of the characteristics of an electrical medical device. In fact, a device could be vulnerable to electromagnetic waves emitted by a wide variety of electrical objects placed in the environment of the medical device. This is a major issue for some devices, especially life-saving devices where the patient’s life depends on the electrical medical device working properly. Let LNE/G-MED’s Guide to Electromagnetic Compatibility light the way to your electrical medical device’s CE marking. LNE/G-MED’s in-house EMC testing experts wrote this guide in order to help clients navigate through the electro-magnetic compatibility testing that the European Directives require. To place an electro-medical device on the European market, a manufacturer must both perform electro-magnetic compatibility and safety testing. This is to ensure the safety of the device and that the patient will realize the device’s maximum benefit. LNE/G-MED’s Guide to Electromagnetic Compatibility is comprehensive and extremely useful for an electrical medical device manufacturer to gain CE marking for their device. The guide includes:
To get your FREE Guide, just complete the information below. Please be sure to include a valid email address so that we can send you your FREE Guide to Electromagnetic Compatibility. |





- Progress Report - News
- MD Revisions Draft Amendments
- MD Classifications
- ISO 14971:2012
- MDD Revision: Actors, Roles and Responsabilities
- WEEE2 Directive
- Maintaining Compliance
- Revisions to the MDD
- ISO 13485 and FDA
- Controlling Outsourced Processes
- The Notified Body’s Role in Medical Device Certification
- EC Publishes E-Labeling Regulation
- IVD Updates
- Post-Market Phase
- IEC 60601 3rd Edition
- Tech File Evaluation
- Clinical Evaluation
- Recast of IVD Directive
- Own Brand Label Devices
- Software Engineering
- Med. Device Packaging
- Single Use Devices
- Usability Engineering
- FDA Use of ISO 13485
- Risk Management
- IVD Directive
- Switching Notified Body
- 60601 3rd Edition Status
- Regulatory News
- Ask Our Experts
- Free Guide: CE Marking
- Free Guide: IEC 60601 3rd Edition
- Free Guide: EMC Testing
- Free Guide: Brazil MD Approval
- Free Guide: Japan MD Approval
- Free Guide: IVD
- Technical FAQs
- Progress Report - News





