European Authorised Representative
Medical device manufacturers without a physical presence in Europe are required to appoint a European Authorised Representative. For EU MDR & IVDR Medical Device CE Marking, an EU Representative is required. EC Rep can be used on any type of medical device.
On device information panels, the name and contact details of the EU Representative must be visible. A European Representative should be selected based on their knowledge and experience with medical device regulations and related regulatory requirements.
Table of Contents
European Authorised Representative Must For MDR & IVDR Compliance
Article 11 section 1: Where a manufacturer is not established in a Member State, the device may only be placed on the EU market if the manufacturer designates a sole authorised representative
Article 11 section 2 states:
- Shall be valid only when accepted in writing by EU AR
- Shall be effective at least for all devices of the same generic device group
- AR shall perform the tasks specified in the mandate agreed
- AR shall provide a copy of the mandate to the Competent Authority upon request
Article 11 section 3 :
(a) Mandate shall require the EAR to Verify DoC and Technical File and confirm appropriate conformity assessment performed
b) Keep available a copy of Technical Documentation, DoC, and NB certificates at the disposal of the Competent Authority >10 / 10 years after the last placing on the market or >15 years for implantable devices
c) Register with SRN, within one week of any change maintain, re-confirm accuracy in the first year, and then every second year also check for correct UDI core data elements assigned / Entered Basic UDI-DI
d) Provide information/documentation to Competent Authority on request to demonstrate conformity in requested language
e) Forward to Manufacturer Competent Authority’s request for samples/access to a device and verify samples/access given
f) Cooperate with Competent Authorities in any preventive/corrective action to eliminate/mitigate risk
g) Immediately inform the Manufacturer about complaints and reports from healthcare professionals, patients, and users about suspected incidents
h) Terminate mandate if Manufacturer acts contrary to its obligations under this Regulation (inform Member State & Notified Body)
Role Of European Authorised Representative
The main roles and Duties of European Authorized Representative by Law are the following
- Authorization to place its name, address, and contact on device labels.
- Acting as your primary contact point for the EU Authorities and NB
- Register your devices with the Authorities before they are marketed.
- Make technical file readily available for the European Competent Authorities
- Notification of serious device incidents to the Competent Authorities
- Assistance with technical documentation or Clinical Evaluation Report
- Guidance on medical device Risk Analysis
- Device compliance with the MDR 2017/745 and IVDR 2017/746.
- Immediate notification of device incidents.
EUDAMED is known as European Databank for Medical Devices, which came into force in May 2011. EUDAMED is enforced for strengthening surveillance and transparency with regards to medical devices placed on the European market. EUDAMED acts as a central repository for information on market surveillance exchanged between the EU commission and national competent authorities.
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European Free Sale Certificate
As the EU Requirements are challenging, various governments worldwide require foreign manufacturers to provide a Certificate of Free Sale (CFS) or Free Sales Certificate (FSC) showing that their products are approved for sale in Europe. I3CGlobal organizes the Free Sale certificate from the EU Competent Authorities to all our existing customers. Free Sales Certificate can only be obtained on your behalf by your current European Authorised Representative or UK Responsible Person.
In order to obtain a Free Sales Certificate, the following
- Mutually Signed EAR Agreement with us
- Technical File
- Complete test reports for Class 1 Devices
- EU Registration Document, If completed
- EUDAMED Registration & SRN Number
Yes. Latest MDR Technical File with updated latest test reports and Signed DOC for self Certified Class I devices. Other devices NB issued CE Certificate and latest technical file is to be submitted.
Yes, we do.
Yes, we do support.
Annual fees payment to EU Representative office
Send device details and DOC to EU Representative to draft the agreement
Client review the draft and confirm the acceptance
Mutually sign the agreement
Send CE Certificate to EU representative
Send Technical File to EU Representative
You choose an EU Authorized Representative that is experienced and well versed in the areas of Medical Devices and related regulatory requirements.
Then the manufacturers draw up an agreement clearly outlining the essential duties of the Authorized Representative in accordance with the requirements in the MDR or IVDR.
Actor Registration Module will become available 2021 March to acquire a Single Registration Number (SRN) for declarations of conformity and certificates.
Manufactures will be able to submit UDI information to EUDAMED from 2021 May
Full fledged EUDAMED Launch expected on May 2022
EUDAMED Device Registration period of 18 months for Legacy, MDR, and IVDR devices during 2022 May – 2023 November.