Freiverkaufszertifikate für aktive Medizinprodukte beantragen
Inhalt
Begriffe im Kontext
- Feststellung der geltenden Normen, technischen Spezifikationen und Zertifizierung der Produkte
Fachlich freigegeben am
Fachlich freigegeben durch
As a manufacturer of active medical devices or its authorized representative, you can apply for the issue of a certificate of free sale for export purposes. This certificate of free sale confirms the marketability of the products in question within the EU.
Are you responsible for placing a medical device on the market and would like to export it outside the Union? Then the relevant competent authority will issue a certificate at your request.
This certificate certifies that the product may be traded in the Union.
- Declaration of conformity of the medical device concerned
- Certificate(s) from the notified body(ies) of the medical device concerned
- Certification of the manufacturer's quality management by a notified body
- Product list in accordance with the MDR
- Your establishment is located in the area of responsibility of the relevant authority and you are registered in Eudamed.
- Your medical devices concerned are registered in DMIDS.
- There are no known concerns on the part of the authority.
- Current documentation of the medical devices concerned is available.
- You submit your application.
- The competent authority checks the documents.
- The competent authority may request additional documents. additional documents.
- If all requirements are met, the competent authority issues the certificate of free sale.
Objection according to Administrative Procedure Act (VwvVfG) against the charging of fees
- Certificates of free sale for export purposes of medical devices Exhibition For medical devices excl. in vitro diagnostics - active
- Certificates of free sale are issued for active medical devices.
- A certificate of free sale can be applied for by manufacturers or EU authorized representatives.
- To apply for a certificate of free sale, the medical devices must meet the legal requirements and be supported by a declaration of conformity.
- Medical devices that have been notified and CE-marked are marketable within the EU and the associated contracting states, i.e. there is no need to issue a certificate.
- The issuing of a certificate of free sale is subject to a fee.
- Responsible: State Office for the Environment (LfU) - Department 2 - Division 25.1
Please contact the State Office for the Environment (LfU) - Department 2 - Division 25.1.
Forms available: No
Written form required: Yes
Informal application possible: Yes
Personal appearance necessary: No
Online services available: Yes