Excellent material compatibility with first-class cleaning activity due to the singular formula based on alkalinity donors, surfactants and enzymes. When used for manual pre-cleaning the cleaner solution does not have to be rinsed off prior to automated reprocessing. No neutralising step necessary for automated reprocessing; therefore short program cycles.

• No hazard label and non-hazardous product
• Viscosity: <10 mPas (concentrate, 20 °C)
• Density: 1,1 g/cm³ (20 °C)
• Titration factor: 0,77

Use suitable dosing devices. Rinse out dosing system including suction hose with water before changing product. Reprocessing should comply with all ordinances pursuant to the regulations on medical devices and should be performed with appropriate validated processes.

Reliably removes residues of dried and denatured blood. Greatly reduces the amount of organic material and prevents the re-deposition of protein residues. Fulfils the current recommendations of the German Robert-Koch-Institute (RKI) for minimising the transmission risk of the new variant of the Creutzfeldt-Jakob disease (vCJD) when reprocessing medical devices. Removes pathogenic prion proteins of
different prion test strains; amongst those the vCJD test strain by >2 lg steps (1%, 55 °C, 10 min.).

Supports the removal of biofilms. Suitable for instruments and utensils made of stainless steel, instrument steel, optics, conventional plastics and the materials of anaesthesia equipment. Anodised aluminium must be tested first for suitability.

Contains <5% non-ionic and anionic surfactants, and also enzymes according to regulation (EC) No 648/2004 on detergents.