The mark consists of The mark consists of the letters "CMDR" in a large teal font, with the phrase "Certified Medical Device Representative" in a smaller blue font directly below "CMDR". To the left of the text is a design featuring colorful human figures in orange, green, teal, and dark blue, forming a circular pattern. In the center of the circle formed by the human figures is a purple clover-like symbol. The purple clover represents the combination of red (the color associated with red surgical caps) and blue (for healthcare), symbolizing the principle of "patients before profits." The circle of human figures represents medical device representatives protecting patients before profits..
The color(s) The mark consists of the letters "CMDR" in a large teal font, with the phrase "Certified Medical Device Representative" in a smaller blue font underneath. The design features colorful human figures in orange, green, teal, and dark blue, forming a circular pattern around a clover-like symbol in the center. The clover pattern is purple, representing the combination of red (the color associated with red surgical caps) and blue (for healthcare), symbolizing the principle of "patients before profits." The circle of human figures represents medical device representatives protecting patients before profits. is/are claimed as a feature of the mark.
The certification mark, as used or intended to be used by persons authorized by the certifier, certifies or is intended to certify that the services provided have met the standards established by the certifier. Specifically, the mark certifies that individuals bearing the mark have demonstrated the requisite level of knowledge, skill, and competency in the field of medical device representation. This includes, but is not limited to, training for ANSI/NEMA SC 1-2020 standards, surgical case setup, surgical case attendance, and surgical tray management. The certification involves rigorous training and assessment processes to ensure that certified representatives are well-versed in the proper use, handling, and reprocessing of medical devices, as well as in compliance with relevant healthcare regulations and standards.