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  • Authorisation of orthopaedic establishments
  • Request initial authorization
9759 - Autorització dels establiments d'ortopèdia Departament de Salut accio
  • What do you need to know?
  • What is it?
  • Who is it for?
  • Deadlines
  • Documentation
  • Requirements
  • Fees
  • Other information

Steps to follow

  1. 1. Apply for authorisation
  2. 2. Check the status of the procedure
  3. 3. Pay the fee
  4. 4. Submit the required documentation
  5. 5. Receive the response from the Administration
  • Go to: Request initial authorization
  • Go to: What is it?
  • Go to: Who is it for?
  • Go to: Deadlines
  • Go to: Documentation
  • Go to: Requirements
  • Go to: Fees
  • Go to: Other information
  • Go to: Steps to follow

Authorisation of orthopaedic establishments

Request initial authorization

WHO
Companies and professionals
HOW
Online
WHEN
At any time

Online Start

Do you need any help?

Find out more

Authorisation of orthopaedic establishments

Request initial authorization

Online Start
WHEN
At any time

WHO
HOW
Companies and professionals Online

Do you need any help?

Do you need any help?

Envia la teva consulta

  • Queries, complaints and suggestions

Support to processing

  • Support to processing
  • 012 Telephone
  • Telèfon 012

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Regulation

  • DECRET 179/2010, de 23 de novembre, pel qual s'estableixen els requisits tecnicosanitaris per a l'autorització sanitària de les ortopèdies i dels establiments d'audiopròtesis i se'n regula el procediment d'autorització.

    . Open in a new window. (DOGC  no.  5764  posted  26/11/2010)

What do you need to know?

What is it?

This procedure is intended for orthopaedic establishments and orthopaedic sections within pharmacies in Catalonia to obtain operating authorization from the Department of Health.

These establishments provide orthopaedic medical devices, such as prostheses and orthoses, aimed at compensating for the loss of autonomy, functionality, or physical capacity of users.

 

Attention: If orthopaedic medical devices are dispensed that are custom-made according to a specialist’s prescription, with characteristics designed for a specific patient, this is not the correct procedure. In this case, authorization must be requested for companies that manufacture custom orthoprosthetic products.

 

Applicable regulation

Authority responsible

  • Departament de Salut
  • Servei d'Ordenació i Qualitat Farmacèutiques
Who is it for?
Companies and professionals

To orthopaedic establishments or pharmacies with an orthopaedics section where these products are not custom-made.

 

 

Deadlines

You can submit the application at any time, but you cannot start the activity until you have the authorization.

Documentation
  • Plan of the establishment: Issued and signed by the competent technician.
  • Annex: Responsible declaration of the technical director.
  • Title or official documentation accrediting the professional exercise of the technical director with a minimum of three years of experience as of May 14, 1999. Documents that serve to accredit professional competence:
    • Declaration indicating the establishment of the activity communication, carried out according to Royal Decree 414/1996, of March 1, which regulated medical products, where the person who wants to obtain recognition as a technical director was listed as the responsible technician.
    • Certification from the General Treasury of Social Security, or the mutual society to which they were affiliated, indicating the company, the labour category (contribution group), and the period of employment.
    • Copy of the employment contract or certification from the company where the work experience was acquired, specifying the duration of the contract periods, the activity performed, and the time interval in which the activity was carried out.

Documents

Annex: Declaration of responsibility by the technical director

Requirements
  1. The establishment must be located in Catalonia.
  2. The technical and sanitary requirements established in Annex 1 of Decree 179/2010, of November 23, must be met.
  3. In no case can orthopaedic medical products made to measure according to the written prescription of a specialist, with characteristics designed for a specific patient, be dispensed. In this case, authorization must be requested for companies manufacturing custom orthopaedic products.
Fees

290.8

Complementary information

The amount of this fee is fixed. Check step 3 "Make the payment".

Other information

Validity of the authorization

The authorization is valid for ten years and must be renewed periodically through the specific procedure.

Modifications of the authorization

All modifications of the data contained in the authorization must be requested or communicated through the specific procedure.

Steps to follow

  1. 1

    Step one

    Apply for authorisation

    This procedure can only be completed online.
    If you apply on your own behalf, you must identify yourself using idCAT Mobile  or a digital certificate.
    If you submit the application as a legal entity, a digital certificate of representation is required.

    By Internet

    Application for authorisation of orthopaedic and/or hearing aid practices

    Start . Go to Application for authorisation of orthopaedic and/or hearing aid practices

    How do you complete the procedure?

    • Fill in the online form.
    • Attach the documentation indicated in the Documentation section.
    • Submit the form and sign it digitally.
    • Once you have successfully submitted the form, you will receive a receipt with the procedure’s identification code.

    With this code, you will be able to check the status of your application in the Private Area.

    If any required information is missing or incorrect, the system will notify you before you submit the form.

    In case of an issue during the process:
    Check the alerts and service suspensions. section of the Electronic Office.
    Consult the support website for the procedure.
    If you need help, call 012(free call).

  2. 2

    Step two

    Check the status of the procedure

    You can do it at:

    You can do it at:

    • In the Private Area (with idCAT Mobile or digital certificate)
    • In the Status of my procedures (with the procedure identifier code and your NIF/NIE).
    • Phone 012 (with the procedure identifier code and your NIF/NIE).

    Check more information on How to monitor and check the status of a procedure.

  3. 3

    Step three

    Pay the fee

    You can pay the fee in the following ways:

    You can pay the fee in the following ways:

    • With a bank card 
      • At the time of submitting the form: After submitting it, a link will appear to make the payment with a card.
      • Later:
        • From the Private Area, if you have digital identification.
        • From the Status of my procedures, if you do not have digital identification.
    • With Bizum
    • With a payment letter

    Consult all the information on how to pay a procedure.

    You must make the payment of the fee to continue the procedure.

  4. 4

    Step four

    Submit the required documentation

    Once your application has been reviewed, the Administration may request additional documentation. You can submit it through:

    Once your application has been reviewed, the Administration may request additional documentation. You can submit it through:

    • Private Area(using idCAT Mobile or digital certificate)
    • Status of my procedures(using the transaction identifier code and your DNI/NIF)

    Check the video tutorial on how to submit documents for a request.

  5. 5

    Step five

    Receive the response from the Administration

    When will I receive the response?

    When will I receive the response?

    The maximum period to receive the response is 3 months from the date of entry of the application in the register. If you do not receive any notification within this period nor are you asked to amend the application, it will be considered accepted by administrative silence.

    How will I receive the response?

    You will receive the notification through the e-NOTUM system.

    Can I file an appeal?

    Yes, you have one month to file an appeal, counting from the day you receive the notification. The appeal must be addressed to the Secretary General of the Department of Health.

Update date 01/20/2025

Related procedures

  • Health authorisation of companies manufacturing custom-made orthopaedic medical devices
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