Helps biostimulating laser equipment well on the way
"We found Bolls Rådgivnings- og Testcenter, and liked the concept of a small company with highly specialized employees. They seemed very serious, which is why we sent out the first of our laser devices for testing and prepared the necessary test reports that we could pass on to DGM. (DGM, Danish Approval of Medical Devices, is authorised by the Ministry of The Interior and Health for approval of all annexes to Directive 93/42/EEC on medical devices) as evidence that our devices comply with applicable rules. Among other things, for radiation, EMC and electrical safety", says Arne Grinsted, PowerMedic.
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