Talladium España, S.L.
Spain Last updated 8 Jun 2026
- Devices
- 1,257
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
Catalogue
Scanbody Ref 54.315.222.21-2
Scanbody Ref 54.322.205.31-2
Implant Mount Ref 75.126.017.48-2
Scanbody Ref 54.315.223.21-2
Analog Ref 34.610.178.01-2
Implant Mount Ref 75.123.037.48-2
Implant Mount Ref 75.423.040.48-2
Analog Ref 22.613.004.01-2
Analog Ref 22.614.060.01-2
Abutment (Pom) Ref 21.513.043.01-2
Analog Ref 22.611.090.01-2
Scanbody Ref 53.412.202.01-2C
Analog Ref 22.613.010.01-2
Implant Mount Ref 75.117.037.48-2
Abutment (Pom) Ref PD3OLR330/P
Analog Ref 34.613.242.01-2
Scanbody Ref 54.315.090.21-2
Abutment (Pom) Ref PD3PKR380/P
Scanbody Ref 54.322.181.31-2
Abutment (Pom) Ref PD3OLH410/P
Implant Mount Ref 75.126.178.48-2
Scanbody Ref 54.322.156.31-2
Scanbody Ref 54.315.018.21-2
Scanbody Ref 54.315.003.21-2
Scanbody Ref 54.315.012.21-2
Abutment (Pom) Ref PD3PKH330/P
Scanbody Ref 54.322.210.31-2
Screwdriver Ref DSPDCLH-32
Scanbody Ref 54.322.247.31-2
Analog Ref 22.614.061.01-2
Scanbody Ref 54.315.014.21-2
Analog Ref 22.612.040.01-2
Scanbody Ref 54.322.209.32-2
Analog Ref 22.613.035.01-2
Analog Ref 34.610.222.01-2
Scanbody Ref 54.322.195.31-2
Scanbody Ref 54.315.121.21-2
Adaptor Ref 49.604.000.04-2
Analog Ref 34.612.233.01-2G
Abutment (Pom) Ref 21.512.042.01-2
Scanbody Ref 54.315.027.21-2
Analog Ref 22.614.057.01-2
Analog Ref 34.612.181.01-2
Abutment (Pom) Ref 21.523.067.01-2
Analog Ref 34.312.209.02-2
Screwdriver Ref 43.624.201.02-2
Scanbody Ref 54.315.182.21-2
Scanbody Ref 52.415.114.01-2
Scanbody Ref 52.415.106.01-2
Scanbody Ref 52.415.105.01-2
Showing 1,101-1,150 of 1,257
EUDAMED certificates
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.
Information
- Address
- 17, C/ Virginia Woolf, LLEIDA, Spain
- Website
- dynamicabutment.com
- [email protected]
- PRRC contact
- NÚRIA CARCELLER
- EUDAMED SRN
- ES-MF-000004601