Pro3dure GR-10 MSI Guides — 3D Anti-Biofilm Resin for Orthodontic Splints

Description

The resin printodent® GR-10 MSI guides Pro3dure is a photopolymerizable resin based on functional (meth)acrylic resins, initiators, colorants and stabilizers , with biomimetic solution based on lactams for multi-species inhibition (MSI°). Reduces the formation of unwanted biofilms on orthodontic appliances (e.g. C. albicans / S. mutans ) without microbicidal effect . It is a medical device indicated for the additive manufacturing of orthodontic and dental objects such as splint .

Available in ocean blue (REF: D1000808) in 1 kg pack.

COMPATIBLE WITH DLP/LCD/SLA 3D PRINTERS

MSI GR-10 3D Resin Guides for Orthodontic Splints

3D resin GR-10 MSI guides Pro3dure is a resin for generative manufacturing of orthodontic and dental splints based on image projection systems (≤ 405 nm), with integrated anti-biofilm technology. The formulation guarantees excellent mechanical properties certified according to ISO 20795-2 (dental technology) and low water absorption. The material can be used for building processes with thick layers from 50 to 100 μm .

Recommended minimum wall thickness: 1.5 mm.

Contraindications

MSI GR-10 guide resin is contraindicated:

• If the patient is known to be allergic to any of the ingredients
• For bruxism splint and splints with wall thickness ≤ 1.5 mm
• For prosthetic bases
• For any application that does not fall within the indicated indication

Main advantages:

• ✅ MSI Anti-Biofilm Technology — multi-species inhibition ( C. albicans / S. mutans ) without microbicides
• ✅ Low water absorption (≤ 32 µg/mm³) and solubility (≤ 5 µg/mm³) — ISO 20795-2
• ✅ High hardness (> 80 Shore D) and flexural strength (≥ 50 MPa)
• ✅ Finishing by polishing for optimal hygiene
• ✅ Compatible with CAD software (e.g. exocad) and Pro3dure post-curing hardware (CD-1, CD-2)
• ✅ Compatible with printers DLP / LCD / SLA (≤ 405 nm)

Specifications

* data from representative sample measurements in Pro3dure internal quality control — ** according to internal specifications — *** ISO 20795-2 (dental technology)

Instructions for use

The bottles of MSI GR-10 resin guides must be Shake well before use .

Make sure the resin is at the appropriate operating temperature. If possible, always keep a bottle in the production unit to avoid temperature differences during refilling.

Carefully pour the resin into the projection unit's tank. Bubbles can be removed with a clean spatula or by using the recoater routine.

1. Prepare the data (CAD & build preparation)
2. Choose the parameters process (build style, etc.)
3. Transfer data to the 3D printer
4. Prepare the print — shake the bottle
5. Fill the tray of the device resin
6. Start printing and build the components
7. Parts cleaning : IPA ≥ 97% or equivalent agent — approx. 4 min. in an ultrasonic bath (pre-cleaning is recommended)
8. Drying : until there are no IPA residues
9. Post-curing (4 min.) : Inert atmosphere recommended — use a suitable light-curing device (e.g. CD-1, CD-2 from pro3dure medical)
10. Finish : polishing of the splints

Important

To avoid harmful effects on the quality of the material, never expose the liquid material to irradiation .

Deviations from the manufacturing process described may lead to different mechanical and optical properties of the MSI GR-10 resin guides.

Ensure the use of personal protective equipment during processing: butyl rubber gloves (EN ISO 374), goggles with side protection, protective clothing.

Caution : Cured resins are chemically resistant—avoid staining clothing! Avoid contact with skin and eyes. In case of accidental contact, rinse with plenty of running water; consult a doctor if necessary.

The batch number and the expiration date are indicated on each package — do not use the product after the expiry date.

⚠️ Reporting obligation : In accordance with the EU Medical Device Regulation, users and patients are obliged to report any serious incidents occurring in relation to this medical device to the manufacturer and the competent authority of the country in which they occurred.

CLP Classification (EC Reg. 1272/2008) : Skin Irrit. 2 (H315), Eye Irrit. 2 (H319), Skin Sens. 1 (H317), STOT SE 3 (H335).