Name and address of the notified bodie	Responsible for the following products	Responsable for the following procedures/modules	Annexes/articles of the directives
TÜV CERT ZERTIFIZIERUNGSGEMEINSCHAFT e. V. Reuterstrasse, 161 16153113 Bonn GERMANY T : 00 49 228 91481 40 F : 00 49 228 91481 44 URL : Email :	Active medical devices : devices to ascertain vital functions equipment for extracorporeal circuits, infusions and haemophoresis anaesthesia devicse, incubators, respirators and oxygen therapy equipment surgical equipment and ancillary surgical equipment imaging equipment : with ionizing radiation with non-ionizing radiation stimulation devices radiotherapy devices : with ionizing radiation with non-ionizing radiation ophtalmological devices dental equipment protheses and rehabilitation devices disinfection and sterilization equipment	Full quality assurance Production quality assurance Product quality assurance	Annex II Annex V Annex VI

0298 - NOTIFIED BODY (UNDER DIRECTIVE 90/385/EEC Active implantable medical devices)

Name and address of the notified bodie	Responsible for the following products	Responsable for the following procedures/modules	Annexes/articles of the directives
TÜV CERT ZERTIFIZIERUNGSGEMEINSCHAFT e. V. Reuterstrasse, 161 16153113 Bonn GERMANY T : 00 49 228 91481 40 F : 00 49 228 91481 44 URL : Email :	All active implantable medical devices	Full quality assurance Production quality assurance	Annex II Annex V