EUDAMED update: Sep 28, 2025

Spineway

FR-MF-000015893

Active

Address: Allée du moulin berger, 7 69130 Ecully
Role: Manufacturer
Date of registration: Nov 3, 2021
Country: France

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Spineway is a medical device manufacturer registered in EUDAMED. Headquartered in Ecully, France. Explore the regulatory profile, devices and certificates on MD Atlas.

Role
Country
Date of registration
Address

EUDAMED update: Sep 28, 2025

Spineway

FR-MF-000015893

Active

Address: Allée du moulin berger, 7 69130 Ecully
Role: Manufacturer
Date of registration: Nov 3, 2021
Country: France

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

Spineway is a medical device manufacturer registered in EUDAMED. Headquartered in Ecully, France. Explore the regulatory profile, devices and certificates on MD Atlas.

About Spineway

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-MF-000015893
Role: Manufacturer
Country: France
Organization name: Spineway
EU VAT number: FR96484163985
EORI: FR48416398500035
Trade register: Lyon
Date of registration: Nov 3, 2021

Contact details for Spineway

Phone: +33 4 72 77 01 52
Email: quality@spineway.com
Website: www.spineway.com
Address: 7, ALLÉE DU MOULIN BERGER 69130 ECULLY 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 Spineway

AHADDAD Sabina
All
Hidden
BAUNEAU Vanessa
Substitute for : (a) | the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; b) | the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) | the post-market surveillance obligations are complied with in accordance with Article 10(10);c (d) | the reporting obligations referred to in Articles 87 to 91 are fulfilled;
Hidden
REYMOND Amélia
Substitute for : b) | the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (d) | the reporting obligations referred to in Articles 87 to 91 are fulfilled;
Hidden

Certificate health for Spineway

No certificates registered for this manufacturer.

Device catalog for Spineway

No devices registered for this manufacturer.

Device families (Basic UDI-DI) of Spineway

No device families registered for this manufacturer.

About Spineway

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-MF-000015893
Role: Manufacturer
Country: France
Organization name: Spineway
EU VAT number: FR96484163985
EORI: FR48416398500035
Trade register: Lyon
Date of registration: Nov 3, 2021

Contact details for Spineway

Phone: +33 4 72 77 01 52
Email: quality@spineway.com
Website: www.spineway.com
Address: 7, ALLÉE DU MOULIN BERGER 69130 ECULLY 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 Spineway

AHADDAD Sabina
All
Hidden
BAUNEAU Vanessa
Substitute for : (a) | the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; b) | the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (c) | the post-market surveillance obligations are complied with in accordance with Article 10(10);c (d) | the reporting obligations referred to in Articles 87 to 91 are fulfilled;
Hidden
REYMOND Amélia
Substitute for : b) | the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; (d) | the reporting obligations referred to in Articles 87 to 91 are fulfilled;
Hidden

Approved members

3 approved members

Statistics for Spineway

0Total Devices

0Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

0Countries

Certificate health for Spineway

No certificates registered for this manufacturer.

Device catalog for Spineway

No devices registered for this manufacturer.

Device families (Basic UDI-DI) of Spineway

No device families registered for this manufacturer.

Spineway

Spineway

About Spineway

Contact details for Spineway

Competent authority

Officers and regulatory representatives of Spineway

Certificate health for Spineway

Related documents

Device catalog for Spineway

Device families (Basic UDI-DI) of Spineway

Related searches

About Spineway

Contact details for Spineway

Competent authority

Officers and regulatory representatives of Spineway

Approved members

Statistics for Spineway

Certificate health for Spineway

Related documents

Device catalog for Spineway

Device families (Basic UDI-DI) of Spineway

Related searches

Approved members

Statistics for Spineway