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Talladium España, S.L.

Spain Last updated 8 Jun 2026

Devices
1,257
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue1,257

Page 15 of 26

  • TiBase® Ref 31.323.015.08-2

    Class IIb EUDAMED Active

  • Screw Ref 41.316.078.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 35.323.022.21-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.303.186.03-2

    Class IIb EUDAMEDFDA UDI Active

  • TiBase® Ref 35.313.004.21-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.323.024.24-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.323.223.02-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.302.102.04-2

    Class IIb EUDAMED Active

  • Screw Ref 41.316.064.01-2

    Class IIb EUDAMED Active

  • Screw Ref 41.314.039.32-2

    Class IIb EUDAMED Active

  • Screw Ref 40.314.007.01-2

    Class IIb EUDAMED Active

  • Impression Coping Ref 29.301.000.14-2

    Class I EUDAMED Active

  • DAS Multi-Unit Ref 42.300.152.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.202.01-2C

    Class IIb EUDAMED Active

  • Screw Ref 44.318.068.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 35.324.028.21-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.323.017.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.324.091.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.312.038.21-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.310.135.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.169.22-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.303.083.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.047.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 35.322.209.21-2

    Class IIb EUDAMEDFDA UDI Active

  • DAS Multi-Unit Ref 42.303.186.05-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.314.046.21-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.322.231.01-2G

    Class IIb EUDAMED Active

  • TiBase® Ref 35.321.090.21-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 48.312.029.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.313.010.01-2

    Class IIb EUDAMED Active

  • Screwdriver Ref 43.634.201.01-2

    Class I EUDAMED Active

  • TiBase® Ref 35.312.003.21-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 62.302.138.06-2

    Class IIb EUDAMED Active

  • Screw Ref 40.316.007.03-2

    Class IIb EUDAMED Active

  • Screw Ref 41.318.079.01-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.303.017.04-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.303.091.01-2

    Class IIb EUDAMEDFDA UDI Active

  • DAS Multi-Unit Ref 42.302.257.02-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.312.033.23-2

    Class IIb EUDAMED Active

  • Scanalog Ref 23.414.262.01-2

    Class I EUDAMED Active

  • TiBase® Ref 35.311.090.21-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 48.312.029.03-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.310.196.03-2

    Class IIb EUDAMED Active

  • Screw Ref 41.315.078.01-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 61.303.015.04-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 48.312.119.03-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 42.302.033.04-2

    Class IIb EUDAMEDFDA UDI Active

  • Screw Ref 41.316.068.01-2

    Class IIb EUDAMED Active

  • TiBase® Ref 31.320.229.01-2

    Class IIb EUDAMED Active

  • DAS Multi-Unit Ref 61.302.102.03-2

    Class IIb EUDAMED Active

Showing 701-750 of 1,257

EUDAMED certificates1

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.

Information

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