Ready-to-use disinfectant for surgical and medical instruments

NOSOPROTECT 100 is a ready-to-use disinfectant.

It drastically removes organic residues and prevents corrosion and discoloration of instruments.
It is suitable for the cleaning of all types of medical and surgical instruments such as forceps, scissors, needles, mirrors, scalpels, blades, etc …

It is used for cleaning and disinfection in ultrasonic bath, in immersion bath or by conventional hand washing.

NOSOPROTECT 100 does not contain phenols, aldehydes, chlorine or EDTA.


  • Ready-to-use solution
  • Drastically removes organic residues
  • Use in immersion bath or ultrasonic bath
  • Prevents corrosion and instruments discoloration
  • Bactericidal, yeasticidal, tuberculocidal, mycobactericidal
  • Virucidal (HBV, HIV, HCV, Herpes, Vaccinia, BVDV, Vaccinia
    Influenza, Εbola, Coronavirus)

Microbiological efficacy

NOSOPROTECT 100 - 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

Ultrasonic bath

NOSOPROTECT 100 can be used in all common types of ultrasonic baths.

NOSOPROTECT 100 - Ready-to-use instrument disinfectant


  • 5 litre canister (Ref. 20008)

Physical properties

  • Appearance: Light blue solution
  • Density: 0.99 g/cm3 at 20˚C
  • pH: 9.5-11.0 at 20˚C
  • Odour: Neutral
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: According to OCDE 301D


NOSOPROTECT 100 is compatible with most materials such as stainless steel, aluminium, glass, ceramics, hard plastics, ebonite, etc … NOSOPROTECT 100 is not compatible with disinfecting preparations containing aldehydes.


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

NOSOPROTECT 100 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 Certification
  • Approved by the General Chemical State Laboratory
  • CE mark according to the medical devices Directive
    (Directive 93/42/EEC)
  • Medical device class IIb