Do you work with medical devices?
Do you work using medical devices? Our worldwide standards comply with the national and international requirements listed below and help manufacturers and care institutions and observe these.
Check our overview with deadlines (inter)national laws and regulations for medical device manufacturers.
Registering products in the Dutch Implant Registry (LIR)
In order to trace implants in a fast and efficient way, an automated registration of all implants is required. That is why the Ministry of Health, Welfare and Sport has commisioned the development of the Dutch Implant Registry, also called Landelijk Implantatenregister (LIR).
As of January 1st 2019, the registration of implants in the Dutch Implant Registry is legally required.