NOSOFAST TB

Foaming disinfectant spray for medical equipment surfaces

NOSOFAST TB is a foaming disinfectant spray with a broad antimicrobial spectrum of activity. It combines excellent cleaning and disinfecting properties and ensures the protection of patients and staff.

Its alcohol-free formulation is ideal for the rapid disinfection of sensitive medical equipment surfaces, such as incubators, monitors, plexiglass, etc.
It is also suitable for all surfaces of medical equipment such as beds, stretchers, work benches and all other medical devices.

NOSOFAST TB does not leave any residue after drying, is odorless and does not affect the medical equipment.

Properties

  • Bactericidal, fungicidal, tuberculocidal, mycobactericidal
  • Virucidal (HIV, HBV, HCV, Herpes, Vaccinia, BVDV, Influenza, Εbola, Coronavirus…)
  • Virucidal against all enveloped viruses in 2 minutes
  • Does not affect the medical equipment
  • Leaves no residue after drying
  • Does not contain phenols, aldehydes, chlorine or EDTA

Microbiological efficacy

NOSOSEPT 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

NOSOFAST TB - Foaming disinfectant spray for medical equipment surfaces

Packaging

  • 1litre spray bottle. (Ref. 20042)
  • 5 litre canister. (Ref. 20043)

Physical properties

  • Appearance: Transparent solution
  • Density: 0.99 g/cm3 at 20˚C
  • pH: 9.5-10.5 at 20˚C
  • Odour: Neutral
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: According to OCDE 301D

Composition

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

NOSOFAST TB 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