R
Hi All
I wonder if anyone can help?
I am trying to find out what need to be done to allow our medical device (Class I and IIb) products to be elligible for reimbursement in europe? Specifically I am currently looking for information for the following countries:
If there isn't information directly available, does anyone know which government agency (or equivalent) to contact to obtain further information.
I am sepcifically wondering how to get our devices onto any appropriate 'listings', how long this takes, what information (eg technical data) is required etc.
Can anyone help?
Many thanks



I wonder if anyone can help?
I am trying to find out what need to be done to allow our medical device (Class I and IIb) products to be elligible for reimbursement in europe? Specifically I am currently looking for information for the following countries:
- Germany
- Belgium
- Spain
- Italy
- France
If there isn't information directly available, does anyone know which government agency (or equivalent) to contact to obtain further information.
I am sepcifically wondering how to get our devices onto any appropriate 'listings', how long this takes, what information (eg technical data) is required etc.
Can anyone help?
Many thanks