 |
mdi europa | Authorized Representative | CE Marking | European Authorized Representative Services For Medical Devices
IVDD, MDD, CE Mark, ISO 9000, IVDD, Authorized Representative, authorised representative, regulatory affairs, mdd 92/43 EEC as amamded by 2007/47/EG or Directive 98/79/EC, ivdd, mdd, AIMDD, aimdd, medical device directive, medical devices, ce mark, european regulatory affairs, iso 9000, en 46000, responsible person, authorized address, in vitro, regulatory affairs, safety officer, CE mark, CE Certification, Medical Device standards, Medical Device Labelling, FDA,MDR, Free Sales Certificate
Mdi-europa.com ~
Site Info
Whois
Trace Route
RBL Check
|