Densitas Inc.’s quality management system has been registered by Intertek, an MDSAP recognized auditing organization, as conforming to the requirements of
Densitas’ quality assurance system also meets the requirements of Directive 93/42/EEC on Medical Devices, Annex II excluding (4) by Intertek Semko AB Box 1103, SE-164 22 Kista, Sweden.
Current Global Regulatory Clearances for Densitas Products
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Canada
USA
UK
