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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USA
UK
Canada
