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ONCOlog Medical QA AB
Vallvägen 4B, SE-756 51, Uppsala, Sweden
PHONE: +46 18-19 45 65
FAX: +46 18-30 06 85
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CE Notified Body DGM, Denmark 0543 I ISO 13485:2003 International Standard specifies the quality system requirements for the design/development, production and, when relevant, installation and servicing of medical devices. CE Certificate Council Directive 93/42/EEC, Annex II, Section 3.2. Medical Device Directive. FDA. PatLog 1.0 FDA cleared 1/23/2009 K090044. PatLog 2.0 FDA cleared 10/9/2009 K092939. ONCOlog Medical registered for sale in the Russian territory.