DHG RoMedic Mover Plus Gebrauchsanweisung Seite 10

10. Symbols
This product complies with the requirements
of the Medical Device Regulation MDR
2017/745
Medical Device
Caution
Manufacturer information
The device is intended for indoor use
Serial number
11. How to report a serious incident
Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the
MHRA or another competent authority of the country in which the user and/or patient is established.
UK
info@directhealthcaregroup.com
T: +44 (0) 800 043 0881
F: +44 (0) 845 459 9832
Other:
info.export@directhealthcaregroup.com
10
Visual Inspection
Read the manual
Product Code
Batch Code
Maximum patient weight
I F U