We are internationally certified to ensure quality and reliability in manufacturing medical devices.
ISO 13485:2016 is a standard for the design and manufacture of medical equipment. It is an independent standard certification that is generally harmonized with ISO 9001:2015. The standard has been prepared in accordance with the European Commission with a view to the essential requirements of EU directives for medical devices and CE marking. For ARCTIKO , the ISO 14385:2016 is a quality management system ensuring that our products meet the EU directive 93/42/EEC for medical devices.
ISO 9001:2015 is the most widely used International standard in the world. It streamlines and documents ARCTIKO's working processes and ensures that production always meets the high quality expectations of ARCTIKO's partners.
EU directive 93/42/EEC for medical devices & CE marking for Class II equipment.
ARCTIKO is registered and has listed the following medical device with the U.S. Food and Drug Administration for FY 2016 Pursuant to Title 21, 807 et seq. of the United States Code of Federal Regulations.
ARCTIKO products are approved according to the following standard(s): UL 471 issued: 2010/11/24 Ed.: 10 Rev: 2014/11/17 Commercial Refrigerators and Freezers. CSA C22.2#120 Issued: 2013/03/01 Ed: 4 Refrigeration Equipment
EU directive 93/42/EEC for medical devices & CE marking for Class II equipment.
ARCTIKO is registered and has listed the following medical device with the U.S. Food and Drug Administration for FY 2016 Pursuant to Title 21, 807 et seq. of the United States Code of Federal Regulations.
ARCTIKO is registered and has listed the following medical device with the U.S. Food and Drug Administration for FY 2016 Pursuant to Title 21, 807 et seq. of the United States Code of Federal Regulations.
I’m ready to help you if you have any questions. Call me at +1 615 988 7000 or e-mail sales@arctiko.com
