Table of Contents
Advertisement
Full Leg Full Spine DR Retrofit System | Introduction to the Full Leg Full Spine application | 25
Labels
This mark shows compliance of the equipment with Directive
93/42/EEC or with Regulation 2017/745 (for European Un-
ion).
This mark indicates that the equipment has a Type B applied
part
Date of manufacture
Manufacturer
Medical device
Serial number
Unique device identifier, in text format and in machine reada-
ble format
The most recent version of this document is available on
www.agfahealthcare.com/global/en/library/index.jsp
c NRTL us label
• certified according Standard AAMI ES60601-1 (US)
• certified according Standard CAN CSA 22.2 no. 60601-1:14
(Canada)
Pinch Points
Read and understand all instructions and warning labels in the
product documentation before using the equipment. Keep man-
ual for future reference.
No stepping on surface.
http://
0326A EN 20211014 1141
Advertisement
Table of Contents
