Skip to content

Talladium España, S.L.

Spain ES-MF-000004601 Last updated 8 Jun 2026

Devices
991
Registries
EUDAMED
FDA recalls
0

Catalogue991

Page 1 of 20

  • TiBase® Ref 31.322.102.21-2

    Class IIb EUDAMED Active

  • Screw Ref 40.320.007.03-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.006.04-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.302.050.01-2

    Class IIb EUDAMED Active

  • STD Multi-Unit 0° Ref 46.303.203.02-2C

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.038.21-2

    Class IIb EUDAMED Active

  • Scanbody Ref 54.315.088.21-2

    Class I EUDAMED Active

  • DAS Multi-Unit Ref 48.312.004.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.323.125.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.313.210.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.310.136.02-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.302.011.01-2

    Class IIb EUDAMED Active

  • Cylinder Ref 29.503.000.03-2

    Class I EUDAMED Active

  • TiBase® Ref 31.322.197.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.312.075.04-2

    Class IIb EUDAMED Active

  • Screw Ref 40.320.003.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.320.136.04-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 48.312.125.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 35.323.030.22-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.225.21-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.313.039.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.314.005.21-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.075.04-2

    Class IIb EUDAMED Active

  • Screw Ref 41.314.048.33-2

    Class IIb EUDAMED Active

  • Screw Ref 41.318.055.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.312.197.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.323.030.23-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.313.045.21-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.303.012.01-2

    Class IIb EUDAMED Active

  • Screw Ref 41.314.064.02-2

    Class IIb EUDAMED Active

  • Intraoral Adaptor Ref 50.314.052.04-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref 21.524.068.01-2

    Class I EUDAMED Active

  • Scanbody Ref 52.415.110.01-2

    Class I EUDAMED Active

  • TiBase® Ref 31.314.262.01-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.302.169.07-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 62.302.182.04-2

    Class IIb EUDAMED Active

  • Screw Ref 41.318.046.01-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 48.312.015.04-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.303.125.02-2

    Class IIb EUDAMED Active

  • Scanbody Ref 54.315.169.21-2

    Class I EUDAMED Active

  • TiBase® Ref 35.322.033.21-2

    Class IIb EUDAMED Active

  • Analog Ref 22.613.027.01-2

    Class I EUDAMED Active

  • TiBase® Ref 31.314.018.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.311.049.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.003.02-2

    Class IIb EUDAMED Active

  • Abutment (Pom) Ref 21.523.073.01-2

    Class I EUDAMED Active

  • TiBase® Ref 31.323.015.22-2

    Class IIb EUDAMED Active

  • TiBase® Ref 35.313.186.21-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.323.186.21-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 61.302.033.02-2

    Class IIb EUDAMED Active

Showing 1-50 of 991

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

Notified body 0051 1 certificate

  • 145/MDR Supplemented

    Quality management system EU MDR

    Issued
    27 Nov 2025
    Expires
    11 Feb 2029
    Reason
    Add device or group

Related companies

Notified bodies

  • Notified body 0051

What Talladium España, S.L. makes

Talladium España, S.L. manufactures dental scanning components, including intraoral SCANBODY devices for digital dental impressions and analog abutment replicas. Their portfolio also includes IMPLANT MOUNTS for dental implant systems and ABUTMENT (POM) components, which are likely used in prosthetic restorations.

These devices are classified under EU Medical Device Regulations as Class I and Class IIa, with all products listed in the EU’s eudamed registry. The company operates under Spanish regulatory jurisdiction as a manufacturer based in Spain.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Talladium España, S.L. manufacture?

Talladium España, S.L. specializes in dental scanning components, primarily intraoral SCANBODY devices used for digital dental impressions. Their portfolio also includes ANALOG abutment replicas, IMPLANT MOUNTS for dental implant systems, and ABUTMENT (POM) components, which are likely used in creating prosthetic restorations. These devices support digital workflows in dentistry, particularly for implantology and crown/bridge fabrication.

Where is Talladium España, S.L. based, and under which regulatory jurisdiction do its devices operate?

Talladium España, S.L. is based in Spain (ES), meaning its devices fall under the regulatory oversight of the European Union’s Medical Device Regulations (MDR). As a Spanish manufacturer, compliance with EU requirements—such as mandatory listing in eudamed—applies to all its products.

Which regulatory registries list Talladium España, S.L.’s devices?

All of Talladium España, S.L.’s devices are listed in the EU’s eudamed registry, which is the official database for medical devices under the EU Medical Device Regulations (MDR). This registry ensures transparency and traceability of devices marketed within the European Economic Area.

How are Talladium España, S.L.’s devices classified under EU regulations?

Talladium España, S.L.’s devices are classified as Class I or Class IIa under the EU Medical Device Regulations (MDR). The classification depends on factors like intended use, risk level, and interaction with the body. For example, SCANBODY devices (used for digital impressions) are typically Class I, while ABUTMENT (POM) components—due to their role in prosthetic restorations—may fall under Class IIa due to higher risk potential.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Spain
Address
17, C/ Virginia Woolf, LLEIDA, Spain
PRRC contact
NÚRIA CARCELLER
EUDAMED SRN
ES-MF-000004601