Highly concentrated disinfectant for medical equipment surfaces

NOSOFLOOR is a high efficacy concentrated solution for the daily cleaning and disinfection of medical device’ surfaces in hospitals, clinics and other health institutions. It is used for the routine disinfection in operating rooms, intensive care units, patient areas, etc.

It combines a broad spectrum of microbicidal properties and a very good cleaning power. It has an excellent compatibility with most materials.

NOSOFLOOR has an excellent compatibility with most materials and does not contain phenols, aldehydes, chlorine or EDTA.


  • Bactericidal, fungicidal, tuberculocidal, mycobactericidal
  • Virucidal (HIV, HBV, HCV, Herpes, Vaccinia, BVDV, Influenza, Εbola, Coronavirus…)
  • Surface disinfectant with excellent cleaning properties
  • Does not affect the medical equipment
  • Leaves no residue after drying
  • Does not contain phenols, aldehydes, chlorine or EDTA

Microbiological efficacy

NOSOFLOOR - 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


NOSOFLOOR is compatible with most materials such as stainless steel, aluminum, glass, ceramics, hard plastics, linoleum, ebonite, etc.

NOSOFLOOR - Highly concentrated disinfectant for floors and surfaces


  • 5 litre canister (Ref. 20025)
  • Dosing pump for 5 litre canister (Ref. 20023)

Physical properties

  • Appearance: Transparent light pink 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: Natural eucalyptus fragrance
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: according to OCDE 301D


Didecyldimethylammonium chloride, N- (3-aminopropyl) -N dodecylpropano-1,3-diamine, isopropanol, non ionic surfactants <5%, corrosion inhibitor, anti-foaming agent, excipients.

NOSOFLOOR is manufactured in Greece. MEDALKAN satisfies the requirements of ISO 9001:2015 for quality management system and the requirements of ISO 13485:2016 for the design and manufacture of medical devices.

ISO Certification
  • CE mark according to the medical devices Directive
    (Directive 93/42/EEC)
  • Medical device class IIa