VarseoWax Surgical Guide

The resin for 3D printing of surgical guides and placement aids for implant prosthetics

VarseoWax Surgical Guide – Special resin for the 3D printing of drilling templates and placement aids for implant prosthetics with BEGO Varseo S
  • VarseoWax Surgical Guide is a resin which is highly resistant to chemicals; the printed objects can be cleaned and disinfected both conveniently and easily
  • The Varseo system is compatible with all common implant planning systems which export to STL format – this facilitates simple transfers of the data sets and production of the drilling templates
  • The 3D printing parameters are tailored for surgical guides to ensure exact shaping in the area around the drill sleeves and, consequently, precise drill holes as well as optimal accuracy of fit during subsequent insertion in the patient’s mouth
  • Extremely short fabrication times and low material consumption equate to cost-efficient production in the laboratory
  • The CE mark certifies security, efficiency and permanent monitoring of VarseoWax Surgical Guide and stands for excellent cross-batch quality standards of the product
  • Biocompatibility confirmed by an independent institute means safety for patients
  • VarseoWax Surgical Guide satisfies the requirements for a Class I* medical device
Product details
Color blue-transparent
Modulus of elasticity ≥ 1,500 MPa
Density ca. 1.12 g/cm3
Layer thickness 100 μm
Viscosity 1,100 mPa*s
Notched impact strength ≥ 3 kJ/m2
Flexural strength ≥ 50 MPa
Wavelength 405 nm
Availability Contents Presentation Quantity REF
VarseoWax Surgical Guide 1.0 kg bottle 1 41012

How to nest a surgical guide
for 3D printing with the BEGO Varseo (by using the 3Shape CAMbridge software)

BEGO qualifed the following software solutions** for implantat planning since the introduction of the Varseo 3D printing system:

smop – powered by swissmedia
3Shape – Implant Studio™
coDiagnostiX™

3Shape** and dental wings** also quali ed the BEGO Varseo as a valida- ted 3D printer for sugical guides.

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* Class 1 medical device as defined by Directive 93/42/EEC

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