EUDAMED update: Jun 3, 2026

INTERNATIONAL MEDICAL MEDIATION

FR-PR-000016999

System / procedure pack producerActive

Address: RUE DE BESANCON, 6 90000 BELFORT
Role: System / procedure pack producer
Date of registration: Nov 23, 2021
Country: France

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INTERNATIONAL MEDICAL MEDIATION is a system and procedure pack producer registered in EUDAMED. Headquartered in BELFORT, France. Explore the regulatory profile, devices and certificates on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED update: Jun 3, 2026

INTERNATIONAL MEDICAL MEDIATION

FR-PR-000016999

System / procedure pack producerActive

Address: RUE DE BESANCON, 6 90000 BELFORT
Role: System / procedure pack producer
Date of registration: Nov 23, 2021
Country: France

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

INTERNATIONAL MEDICAL MEDIATION is a system and procedure pack producer registered in EUDAMED. Headquartered in BELFORT, France. Explore the regulatory profile, devices and certificates on MD Atlas.

About IMM

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-PR-000016999
Role: System / procedure pack producer
Country: France
Organization name: INTERNATIONAL MEDICAL MEDIATION
EU VAT number: FR79379490956
EORI: FR3794909560065
Trade register: 379490956 RCS Belfort
Date of registration: Nov 23, 2021

Contact details for IMM

Phone: +33 3 84 27 25 22
Email: contact@immfrance.fr
Website: www.immfrance.fr
Address: 6, RUE DE BESANCON 90000 BELFORT 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

Role and obligations in EUDAMED

A producer of systems or procedure packs combines CE-marked devices to place a system or procedure pack on the market under the conditions of Article 22 of the MDR (2017/745).