Acidic Neutralizing Agent and Instrument Renovator

NEUTRALKAN is an acidic detergent. It is a highly concentrated combination of organic and inorganic acids. It removes limescale, rust stains and mineral deposits off the instruments as well as the inside walls of the washer disinfectors.

It can be used:

  • In automatic washers, washer disinfectors or other instrument reprocessing equipment as a neutralising agent of alkaline residues for surgical instruments and glassware.
  • In immersion bath as a powerful instrument renovator. NEUTRALKAN will remove rust stains and restore the initial brilliance of degraded or discoloured instruments.

  • NEUTRALKAN is compatible with stainless steel instruments, ophtalmological instruments, anesthetic equipment, laboratory glassware, hard plastics and all acid resistant medical devices.


    • Restores the initial brilliance of degraded or discoloured instruments
    • Removes alkaline residues, mineral scale and rust stains
    • Restores stainless steel surface finish
    • Keeps the washer disinfector’s chamber clean and shiny
    • Very economical: 0.05% to 0.4% dilution in washers
    • Does not contain any surfactants
    • Prevents corrosion and instruments discoloration


    NEUTRALKAN is compatible with most materials like stainless steel, glass, ceramics and acid resistant materials.
    Material compatibility with sensitive materials should always be checked before use.


    Citric acid, Phosphoric acid > 50%

    NEUTRALKAN - Acidic neutralizing agent for the automated reprocessing of surgical instruments and equipment


    • 5 litre canister (Ref. 20028)
    • 10 litre canister (Ref. 20029)

    Physical properties

    • Appearance: Transparent solution
    • Density: 1.50 g/cm3 at 20˚C
    • pH (1-4 ml/l.): <2 at 20˚C
    • Viscosity: <50 mPas at 20˚C
    • Storage: 5˚C – 35˚C
    • Stability: 3 Years
    • Biodegradability: According to OCDE 301D

    NEUTRALKAN is manufactured in the EU.
    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 Certification

    • Medical device class I
    • CE mark according to the medical devices MDR Regulation (EU) 2017/745