MD Atlas update: Jun 6, 2026

ISAN

FR-AR-000021370

Authorised representativeActive

Address: PLACE DES MARTYRS DE LA RESISTANCE, 24 13090 AIX EN PROVENCE
Role: Authorised representative
Date of registration: Mar 14, 2022
Country: France

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ISAN is an EU authorised representative registered in EUDAMED. Headquartered in AIX EN PROVENCE, France. Explore the regulatory profile, devices and certificates on MD Atlas.

Role
Country
Date of registration
Address

MD Atlas update: Jun 6, 2026

ISAN

FR-AR-000021370

Authorised representativeActive

Address: PLACE DES MARTYRS DE LA RESISTANCE, 24 13090 AIX EN PROVENCE
Role: Authorised representative
Date of registration: Mar 14, 2022
Country: France

Is this your company? Claim it to add your logo, story and links — free.Claim this page

ISAN is an EU authorised representative registered in EUDAMED. Headquartered in AIX EN PROVENCE, France. Explore the regulatory profile, devices and certificates on MD Atlas.

About ISAN

SRN An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor. View in glossary →: FR-AR-000021370
Role: Authorised representative
Country: France
Organization name: ISAN
EU VAT number: FR29753114925
EORI: FR2975311492500021
Trade register: 753114925
Date of registration: Mar 14, 2022

Contact details for ISAN

Phone: +33442672481
Email: europe@matsuda.com
Website: www.matsuda.com
Address: 24, PLACE DES MARTYRS DE LA RESISTANCE 13090 AIX EN PROVENCE FRANCE

Competent authority

Name: Agence Nationale de Sécurité du Médicament et des Produits de Santé
SRN An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor. View in glossary →: FR-CA-008
Phone: + 33 (1) 5587 3000
Email: contact.eudamed@ansm.sante.fr

Officers and regulatory representatives of ISAN

RIDOR Lola
Administrative missions & Customer Service Manager
Hidden

Role and obligations in EUDAMED

An authorised representative is an entity established in the European Economic Area that a manufacturer based outside the EEA appoints to act on its behalf for specified regulatory tasks. Registration in EUDAMED is required under Article 11 of the MDR (2017/745) and Article 11 of the IVDR — règlement (UE) 2017/746.

Non-EU manufacturers represented

No represented manufacturers on record

EUDAMED does not currently list any manufacturer linked to this entity. This is common for recently-registered operators, or where the principal manufacturer recorded the relationship under a different SRN.