medical
For medical product safety in North America, RTL has tested to the following standards:
• UL 2601-1
• CSA C22.2 No. 601.1
For international safety requirements, we have tested to the following standards:
• EN 60601-1
• EN 60601-2-XX
The Medical Directive EMC standards consists of EN 60601-1 and EN 60601-2. Part 1 addresses all medical products, while Part 2 covers specific requirements for particular types of medical devices. Within EN 60601-2-xx, there are over 40 applicable standard variations within medical devices.
Medical EMC testing performed by RTL is performed to EN 60601-1-2. Deviations and/ or additions to the requirements of EN 60601-1-2, as published in the appropriate EN 60601-2-XX, may be applicable to a device.

Visit our main site at www.rheintech.com