• CE 2292

    CE 2292

    It shows the suitability of the covered products according to Medical Device Directive 93/42/EEC. It is given by the notified body which is approved by the European Union. Proles has got CE 2292 mark for its production of sterile products in the first aid kits.



    DIN 13164 Quality Standard is given by DIN (Deutsches Institut für Normung e.V.) for the First Aid Contents. This norm is accepted even by all the European countries.


Proles produces the first-aid kit contents according to quality standard DIN 13164.

  • ECE 2163

    ECE 2163

    Personal Protective Equipment Directive 89/686/EEC Proles Otomotiv is authorized by the European Union under the EN 471 standard control entered into by the Notified Body Personal Protective Equipment Directive 89/686/EEC passing through and within the scope of the Audit Success received the CE Certificate. The organization of this document and reflective vests certified to comply with the European directives and EN 471 Standard.

  • ECE 27R

    ECE 27R

    Manufacturers in the automotive industry should have international quality certificates such as E or ECE, to be in the international markets.

    RDW is one of the most reputable notified bodies that provide this type of quality approvals and certifications.

Proles has been manufacturing warning triangle with E 4 mark which was provided from RDW organizations. (Approval number: E4-27R-032 746)

  • ISO 13485-2003

    ISO 13485-2003

    ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.

  • ISO 9001-2008

    ISO 9001-2008

    ISO 9001:2008 quality standards mean that; there are a set of procedures that cover all key processes in the business; monitoring processes to ensure they are effective; keeping adequate records; checking output for defects, with appropriate and corrective action where necessary; regularly reviewing individual processes and the quality system itself for effectiveness; and facilitating continual improvement.