Registration

Mandatory requirements for registration in the Catalogue:

Entity located in Portugal;
Regularised situation with the Tax and Social Security Authority;
ensure the quality of the product for its intended purpose;
Support products will have to be classified according to ISO 9999:2007 (6 digits);
The entity will be responsible for any inaccurate information, as well as for the possible damages that may cause to third parties;
The entity will be responsible for the content of the information sent to the INR, I.P., as well as for making the information available for updating the data.

NOTES:

The INR, I.P. reserves the right to remove the entity from the Catalogue if there is a substantiated complaint or anomaly in the support products submitted;
The INR, I.P. is responsible for the final validation for adherence to the Catalogue;
The Catalogue is presented in version only online.

Your information

label.registration.form

Name (Required)

Email (Required)

NIF (Required)

Your access data

Username (Required)

password (Required)

Quanto é 1+1 How much is 1+1*

I hereby declare for all due purposes that my tax situation with the Tax and Customs Authority and my social security contributions are regularized.
The statements made are true and do not omit any relevant information. False statements are punishable under the law. (Required)

When registering its products in the National Catalog of Support Products, the Entity declares that:

✓ All medical devices bear CE marking
✓ If your Entity carries out the activity of manufacturing and/or wholesale distribution of medical devices:
- Notified your activity to INFARMED, I.P.,
- Registered all Medical Devices with INFARMED, I.P.

NOTE: INR, I.P. may request proof of the requirements described above at any time. (Required)

* Mandatory field