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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 24 of 26

  • Implant Mount Ref 75.120.004.48-2

    Class IIa EUDAMED Active

  • Analog Ref 34.613.234.01-2G

    Class I EUDAMED Active

  • Scanbody Ref 54.315.251.21-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref PD3PKR425/P

    Class I EUDAMED Active

  • Analog Ref 22.612.021.01-2

    Class I EUDAMED Active

  • Analog Ref 34.614.235.01-2G

    Class I EUDAMED Active

  • Implant Mount Ref 75.120.221.48-2

    Class IIa EUDAMED Active

  • Analog Ref 22.612.003.01-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.037.21-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.153.22-2

    Class I EUDAMED Active

  • Analog Ref 22.614.096.01-2

    Class I EUDAMED Active

  • Analog Ref 22.613.037.01-2

    Class I EUDAMED Active

  • Screwdriver Ref DSPDCLH-24

    Class I EUDAMED Active

  • Scanbody Ref 54.315.087.21-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.170.21-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.126.019.48-2

    Class IIa EUDAMED Active

  • Implant Mount Ref 75.119.037.48-2

    Class IIa EUDAMED Active

  • Extensor Ref 79.600.010.02-2

    Class IIa EUDAMED Active

  • Extensor Ref 79.600.007.02-2

    Class IIa EUDAMED Active

  • Analog Ref 22.613.002.01-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.117.220.48-2

    Class IIa EUDAMED Active

  • Analog Ref 22.613.025.01-2

    Class I EUDAMED Active

  • Analog Ref 34.613.252.01-2G

    Class I EUDAMED Active

  • Implant Mount Ref 75.117.221.48-2

    Class IIa EUDAMED Active

  • Analog Ref 34.613.223.01-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.016.21-2

    Class I EUDAMED Active

  • Analog Ref 34.615.259.01-2G

    Class I EUDAMED Active

  • Scanbody Ref 54.312.210.31-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.419.040.48-2

    Class IIa EUDAMEDFDA UDI Active

  • Scanbody Ref 53.413.203.01-2C

    Class I EUDAMED Active

  • Analog Ref 34.612.202.01-2C

    Class I EUDAMED Active

  • Scanbody Ref 52.415.101.01-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref 21.522.076.01-2

    Class I EUDAMED Active

  • Adaptor Ref 49.604.000.09-2

    Class I EUDAMED Active

  • Scanbody Ref 53.413.264.01-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.111.21-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref PD3OLH330/P

    Class I EUDAMED Active

  • Scanbody Ref 54.315.119.21-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.091.21-2

    Class I EUDAMED Active

  • Scanbody Ref 53.413.025.01-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.017.21-2

    Class I EUDAMED Active

  • Scanbody Ref 54.322.074.31-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref 21.522.072.01-2

    Class I EUDAMED Active

  • Abutment (Pom) Ref 21.512.078.01-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.047.21-2

    Class I EUDAMED Active

  • Scanbody Ref 54.315.096.21-2

    Class I EUDAMED Active

  • Prescanbody Ref 53.412.998.01-2

    Class I EUDAMEDFDA UDI Active

  • Scanbody Ref 53.423.263.01-2C

    Class I EUDAMED Active

  • Analog Ref 22.612.075.01-2

    Class I EUDAMED Active

  • Implant Mount Ref 75.126.016.48-2

    Class IIa EUDAMED Active

Showing 1,151-1,200 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