Surface broad spectrum fast acting disinfection spray

NOSOSEPT 100 is a broad spectrum antimicrobial disinfectant spray specially formulated for the rapid cleaning and disinfection of surfaces of medical devices. Active in 30 seconds, its use after each session prevents cross-contamination between patients.

It is recommended for surfaces of medical devices in direct contact with patients and medical personnel such as trolleys, benches, examination tables, operating room furniture, etc.

NOSOSEPT 100 has excellent disinfectant properties, a mild odor and leaves no residues after drying.


  • Active in 30 seconds
  • Leaves no residue after drying
  • Does not affect the medical equipment
  • Bactericidal, fungicidal, tuberculocidal, mycobactericidal
  • Virucidal (HIV, HBV, HCV, Herpes, Vaccinia, BVDV, Influenza, Εbola, Coronavirus, Rotavirus…)
  • Does not contain phenols, aldehydes, chlorine or EDTA

Microbiological efficacy

NOSOSEPT 100 - Microbiological efficacy

* Including all antibiotic resistant bacteria such as MRSA, Escherichia coli, Klebsiella pneumoniae, Streptococcus pneumoniae, etc.)
(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

NOSOSEPT 100 - Surface broad spectrum fast acting disinfection spray


  • 1 litre spray bottle (Ref. 20003)
  • 5 litre canister (Ref. 20004)

Physical properties

  • Appearance: Transparent solution
  • Density: 0.97 g/cm3 at 20˚C
  • pH: 9.0-9.6 at 20˚C
  • Odour: Mild (alcohol)
  • Storage: 5˚C – 35˚C
  • Stability: 3 Years
  • Biodegradability: According to OCDE 301D


Isopropyl alcohol, didecyldimethyl ammonium chloride,
N- (3-aminopropyl) -N dodecylpropano-1,3-diamine, excipients.

NOSOSEPT 100 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
  • CE mark according to the medical devices Directive
    (Directive 93/42/EEC)
  • Medical device class IIa