CITRALKAN

Acidic Neutralizing Agent for the Reprocessing of Surgical instruments

CITRALKAN is an acidic detergent for the neutralization of alkaline deposits in washer disinfectors and/or acidic pre-cleaning of instruments and laboratory glassware. It support optimized cleaning chemistry and enhanced surface appearance.

CITRALKAN removes limescale, rust stains and mineral deposits off the instruments as well as the inside walls of the washer disinfectors. It is commonly used in washer disinfectors or other instrument reprocessing equipment.

CITRALKAN is compatible with stainless steel instruments, ophthalmological instruments, anaesthetic equipment, laboratory glassware, hard plastics and all acid resistant medical devices.

Properties

  • Removes alkaline residues, mineral scale and rust stains
  • Acidic pre-cleaning of instruments and laboratory glassware
  • Keeps the washer disinfector’s chamber clean and shiny
  • Based on organic acids
  • Very economical: 0,1% to 0,2% dilution
  • Does not contain any surfactants, prevents corrosion and instrument discoloration

Compatibility

CITRALKAN 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.

Composition

Citric acid ≥ 40%, Corrosion inhibitors.

CITRALKAN - Acidic neutralizing agent for the reprocessing of surgical instruments

Packaging

  • 5 litre canister (Ref. 20077)
  • 10 litre canister (Ref. 20078)
  • Dosing pump for 5 litre canister (Ref. 20023)

Physical properties

  • Appearance: Transparent solution
  • Density: 1.15 g/cm3 at 20˚C
  • pH (1-2 ml/l.): inferior to 3 at 20˚C
  • Viscosity: inferior to 10 mPas at 20˚C
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: According to OCDE 301D

Downloads

CITRALKAN – Product Data sheet (PDS)

CITRALKAN – Material safety data sheet (MSDS)

CITRALKAN 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 and CE mark Certifications - MEDALKAN

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