EU Representatives

European Union Authorised Representative
In accordance with Regulation (EU) 2017/745, DETARCOOP MEDICAL has appointed an EU Authorised Representative for the applicable medical devices covered by the mandate.
MDR Article 11 specifically requires a non-EU manufacturer placing devices on the EU market to designate a sole authorised representative, subject to the regulation’s requirements.

EU AUTHORISED REPRESENTATIVE
LORCAN & FYON B.V.
Address:
Europalaan 40
3526 KS Utrecht
The Netherlands
Manufacturer represented:
DETARCOOP MEDICAL
Pakistan
Role:
European Union Authorised Representatives
Certificate of EC Representation.

Information

In compliance with the guidelines provided by the Ministry of Health on advertising relating to medical devices and medical-surgical aids, we inform the private citizen that the contents of these pages are intended exclusively for healthcare professionals. All the contents of the site are of a purely informative nature, aimed at informing healthcare professionals only. All the products displayed on this site and having the nature of, medical devices, as well as all the contents of the site, are not of an advertising nature