Obelis European Authorized Representative Center
"CE Marking Consultants with a Reputation for Excellence"Devices which fall under the directive include:
Any device, apparatus, appliance or material used on human beings for the purpose of diagnosing, treating, preventing, monitoring, or alleviating a person’s condition as well as in conjunction with those who are injured or handicap. A medical device can also be defined in this directive as any of the previously listed in concurrence with conception. If any of these relate to your device, it is classified as a medical device.
Our sister company GiDoS s.p.r.l. provides REACH, WEEE,
RoHS and P&PW compliance services.
Visit GiDoS.net
Directive codes: MSD 2006/42/EC - TSD 2009/48/EC - CPR 305/2011/EU - ATEX 94/9/EC - MVD 2007/46/EC - 90/385/EEC - PED 97/23/EC - R&TTE 1999/5/EC - 93/68/EEC - 2004/108/EC - PPE 89/686/EEC - LVD 2006/95/EC - 76/768/EEC - GPSD 2001/95/EC - IVDD 98/79/EC - MDD 93/42/EEC -
General Sitemap | Sitemap EU Directives | European Directives Articles
Contact Us | Terms & Conditions
Copyright © Obelis SA 2008
Registered Office Address
Av. de Tervuren 34
BTE 44, B-1040 Brussels
Belgium
Tel: +(32) 2 732-59-54
Fax: +(32) 2 732-60-03
mail@obelis.net
Registered Address
Bd Général Wahis 53
1030 Brussels
Belgium
Tel: +(32) 2 732-59-54
Fax: +(32) 2 732-60-03
mail@obelis.net
