TOTOKU displays provide
worldwide medical safety standards
| UL | CE Marking | FDA 510(k) |
| UL (Underwriters Laboratories, Inc.) is an independent nonprofit testing and certification organization established in the United States. TOTOKU medical image displays are certified under UL60601-1, CSA C22.2 N601.1, thus labeled with the UL Listing Marking. | CE Marking is provided for products sold in European countries to indicate that the products conform to the EU Directive. Products from outside the EU sold into the EU market are required to includethis CE Marking. TOTOKU medical image displays are certified under EN60601-1-1 (medical safety standard) and EN60601-1-2 (medical EMC standard) and conform to the Medical Device Directive (MDD), and are labeled with the CE Marking. | 510(k), also known as Premarket Notification, refers to an application submitted to the Food and Drug Administration (FDA). It is an FDAnational standard to allow a determination of the safety, effectiveness, and substantial equivalence of a device to a device already legally on the US market in the past or present. Its strict evaluation covers not only the safety and effectiveness of the device, but also proper labeling, including advertisements. |
