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MD Atlas update: Jun 28, 2026
SE556593070701
SE5565930707
556593-0707
SE-MF-000003568
2 contacts identified
Certificate 28620161156
Manufacturer
Ortivus MobiMed AB
Notified body
Intertek Medical Notified Body AB
2862
Version
1
Valid from
11/28/2023
Valid until
11/27/2028
No devices registered for this manufacturer.