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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 25 of 26

  • Extensor Ref 79.600.009.02-2

    Class IIa EUDAMED Active

  • Analog Ref 34.613.203.01-2C

    Class I EUDAMED Active

  • Extensor Ref 79.600.008.02-2

    Class IIa EUDAMED Active

  • Analog Ref 22.614.028.01-2

    Class I EUDAMED Active

  • Analog Ref 22.613.022.01-2

    Class I EUDAMED Active

  • Analog Ref 34.613.263.01-2C

    Class I EUDAMED Active

  • Implant Mount Ref 75.421.040.48-2

    Class IIa EUDAMEDFDA UDI Active

  • Analog Ref 22.613.263.01-2C

    Class I EUDAMED Active

  • Analog Ref 22.614.058.01-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.124.178.48-2

    Class IIa EUDAMED Active

  • Extractor Ref 49.603.000.02-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.118.037.48-2

    Class IIa EUDAMED Active

  • Implant Mount Ref 75.125.037.48-2

    Class IIa EUDAMED Active

  • Scanbody Ref 54.315.026.21-2

    Class I EUDAMED Active

  • Scanbody Ref 54.312.209.31-2

    Class I EUDAMEDFDA UDI Active

  • Implant Mount Ref 75.124.017.48-2

    Class IIa EUDAMED Active

  • Analog Ref 34.312.210.01-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref PD3OLR410/P

    Class I EUDAMED Active

  • Analog Ref 22.613.041.01-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.121.037.48-2

    Class IIa EUDAMED Active

  • Analog Ref 22.612.026.01-2

    Class I EUDAMED Active

  • Screwdriver Ref 43.618.103.01-2

    Class I EUDAMED Active

  • Handle Ref 49.601.000.05-2

    Class I EUDAMED Active

  • Analog Ref 34.612.182.01-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.420.040.48-2

    Class IIa EUDAMEDFDA UDI Active

  • Scanbody Ref 53.414.204.01-2C

    Class I EUDAMED Active

  • Analog Ref 22.312.209.01-2

    Class I EUDAMED Active

  • Analog Ref 22.613.073.01-2

    Class I EUDAMED Active

  • Scanbody Ref 54.322.146.31-2

    Class I EUDAMED Active

  • Analog Ref 22.612.033.01-2

    Class I EUDAMED Active

  • Analog Ref 22.612.023.01-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.092.21-2

    Class I EUDAMED Active

  • Analog Ref 34.612.251.01-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref 21.523.054.01-2

    Class I EUDAMED Active

  • Screwdriver Ref 43.321.320.01-2

    Class I EUDAMED Active

  • Scanbody Ref 52.415.107.01-2

    Class I EUDAMED Active

  • Mount Extractor Ref 79.300.001.03-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.417.040.48-2

    Class IIa EUDAMEDFDA UDI Active

  • Scanbody Ref 54.327.247.31-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.028.21-2

    Class I EUDAMED Active

  • Analog Ref 22.610.159.01-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref 21.523.062.01-2

    Class I EUDAMED Active

  • Anchor Screw Ref 79.300.012.02-2

    Class I EUDAMEDFDA UDI Active

  • Scanbody Ref 54.315.011.21-2

    Class I EUDAMED Active

  • Screwdriver Ref 43.621.316.01-2C

    Class I EUDAMED Active

  • Analog Ref 22.612.001.01-2

    Class I EUDAMED Active

  • Screwdriver Ref 43.322.316.01-2

    Class I EUDAMEDFDA UDI Active

  • Abutment (Pom) Ref PD3PKR330/P

    Class I EUDAMED Active

  • Abutment (Pom) Ref PD3PKH380/P

    Class I EUDAMED Active

  • Analog Ref 34.613.146.01-2

    Class I EUDAMED Active

Showing 1,201-1,250 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