VECTEC is certified according to standard EN ISO 13485: 2012 by the LNE GMED 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 LNE GMED.

Our Quality policy goal :

  • 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.
  • We maintain efficiency of our Quality Management System (QMS).

In particular, all our single-use medical devices are made with recyclable materials, without latex.

To ensure that our medical devices are the best quality possible, we carry out quality controls at every stage in their manufacture.

The main processes are : injection-molding, machining, assembly, packing, sterilization.


GMED-4CO[1] (2)


EN ISO 13485 Certificate EN ISO 13485 Certificate EC Certificate EC Certificate EC Certificate Class Is EC Certificate Class Is