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.
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Our sister company GiDoS s.p.r.l. provides REACH, WEEE, RoHS and P&PW compliance services
Directive codes: 90/385/EEC - CPD 89/106/EEC - PED 97/23/EC - R&TTE 1999/5/EC - 93/68/EEC - TSD 88/378/EEC - MSD 98/37/EC - 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 -
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Tel: +(32) 2 732-59-54
Fax: +(32) 2 732-60-03
mail@obelis.net
