Active implantable medical devices
Directive 90/385/EEC
amended by directive 2007/47/CE

Status of LNE/G-MED: notified body
Accreditation number: 0459
Services provided by LNE:
LNE will:
provide expert advice concerning classification of devices and certification procedures,
issue the certificates required for CE marking,
carry out an EC examination of design files,
carry out EC type-examinations,
perform conformity tests to harmonized European standards or other standards,
perform quality system audits in accordance with the Directive Annexes,
assess clinical data in consultation with hospital experts

Scope:
Active implantable medical devices
LNE/G-MED strengths:
LNE/G-MED issues certificates for all conformity procedures and all medical devices covered by the Directive.
Technical file examinations and audits are performed by qualified experts who are specially trained for each category of devices.
Quality system audits are performed anywhere in the world.
LNE/G-MED is actively involved in the work of NB-MED (Coordination of Notified Bodies for Medical Devices) and European standardization bodies.

Additional services:
one-stop auditing for ISO 9001, ISO 13485 and mandatory certification
French NF Médical mark issued
training (in French)
one-day technical information sessions (in French)

Recognition by third-party bodies:
LNE/G-MED is approved by the following accreditation bodies:
- COFRAC (France) for all voluntary company certification
- SCC (Canada) for ISO 13485 certification (CMDCAS programme)

Contact: Customer service