ReSound OMNIA 312 User Manual page 80

Manufacturer according to EU Medical
Device Regulation 2017/745:
GN ReSound A/S
Lautrupbjerg 7
DK-2750 Ballerup
Denmark
resound.com
CVR no. 55082715
Any serious incident that has occurred in relation to the device should be reported to the legal manufacturer GN ReSound
A/S and the competent authority of the EU Member State in which the user and/or patient is established.
Manufacturer according to FDA:
GN ReSound North America
8001 E Bloomington Freeway
Bloomington, MN 55420
USA
1-888-735-4327
resound.com
ReSound Government Services
8001 E Bloomington Freeway
Bloomington, MN 55420
USA
1-800-392-9932
resound.com/veterans
Manufacturer according to Health Canada:
ReSound Canada
2 East Beaver Creek Road, Building 3
Richmond Hill, ON L4B 2N3
Canada
1-888-737-6863
resound.com