MEDAPRINT

Concentrated disinfectant for dental impressions

Medalkan > MEDAPRINT

MEDAPRINT is a concentrated solution specially designed for the cleaning and disinfection of dental impressions. It does not contain aldehydes and is very economical.
It does not affect the dimensionnal accuracy of the impressions materials.

Properties

  • Very economical: 1% dilution
  • Action time: 15 minutes
  • Compatible with impressions from alginate, silicone, polyether and hydrocolloids
  • Drastically removes organic residues, saliva and blood
  • Bactericidal, yeasticidal
  • Virucidal (HBV, HIV, HCV,Herpes, Vaccinia, BVDV, influenza, Εbola, Coronavirus…)
  • Tuberculocidal, mycobactericidal
  • Does not contain phenols, aldehydes, chlorine or EDTA

Microbiological efficacy

MEDAPRINT - Microbiological efficacy

  1. DVV: Deutsche Vereinigung zur Bekämpfung der Viruskrankheiten / German Association for the Control of Virus Diseases
  2. RKI: Robert Koch Institute – German Federal Health Authority

Compatibility

MEDAPRINT is Compatible with impressions from alginate, silicone, polyether and hydrocolloids.
MEDAPRINT is not compatible with disinfecting preparations containing aldehydes.

MEDAPRINT - Concentrated disinfectant for dental impressions

Packaging

  • 1 litre bottle with dispenser (Ref. 20015)

Physical properties

  • Appearance: Transparent solution
  • Density: 0.99 g/cm3 at 20˚C
  • pH: 12-12.8 at 20˚C
  • pH (1%): 9.5-10.5 at 20˚C
  • Odour: Neutral
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: According to OCDE 301D

Composition

N- (3-aminopropyl) -N dodecylpropano-1,3-diamine, non-ionic surfactants <5%, isopropanol, excipients.

Downloads

MEDAPRINT – Product information sheet (PIS)

MEDAPRINT – Material safety datasheet (MSDS)

MEDAPRINT is manufactured in Greece. MEDALKAN satisfies the requirements of ISO 9001 for quality management system and the requirements of ISO 13485 for the design and manufacture of medical devices.

ISO 9001, ISO 13485, CE
  • CE mark according to the medical devices Directive (Directive 93/42/EEC)
  • Medical device class IIb