VECTEC is certified according to standards NF EN ISO 9001: 2008 and NF EN ISO 13485 : 2011 by the TÜV Rheinland certifying authority.

VECTEC has obtained the EC mark for its products according to the Medical Devices Directive (appendix II) 93/42 EC by the notification body TÜV Rheinland.

Our Quality policy Our goal is to satisfy our customers and be attentive to their needs. We guarantee quality products for our customers, manufactured according to current standards, and using environmentally friendly materials.

In particular, all our single-use medical devices are made with recyclable materials. To ensure that our medical devices are the best quality possible, we carry out quality controls at every stage in their manufacture: injection-moulding, machining, assembly, packing, and sterilisation.

   ISO 9001            ISO 13485          CERTIFICAT CE      ISO CANADA