Purespace® Machines

PURESPRAY®

Disinfection device for sterilization of the indoor spaces from 10 to 1000m3

Very easy usage

  • Simply enter the volume of the room to be treated.
  • Very little product required: 1ml of product is enough to treat 1m3.
  • No preparation necessary before treatment (except cleaning) and no action required after treatment (no need to wipe surfaces or air the room).
  • Treatment is in two stages: diffusion via Nocospray for a certain time, then contact time for the disinfectant.
  • Stops automatically.

Example of how to use: preventive treatment for a 50m3 room:

  • Diffusion time: 3 min
  • Contact time: 30 min
  • Total time taken for disinfection: 33 min

Technical Characteristics

Electric turbine: 1,100 watts
Speed of rotation: 22,000 rpm
Escape speed of fog: 80 m/sec
Weight: 5,8 kg (Easy to transport)
Available voltage: 115 V/230 V

3 models of Purespray® available depending on the volume to be treated:

  • From 10 to 250m3
  • From 20 to 500m3
  • From 40 to 1,000m3
Manufactured in accordance with ISO 9001.

Purespace® Disinfectants

PURESPACE®

Disinfectant solution is recommended for preventive treatments.

PUREFOOD®

Disinfectant solution is recommended for spaces or surfaces that come into contact with food production or food processing.

Purespace® Micro-organisms tests

Pseudomonas aeruginosa* Candida albicans* Acinetobacterbaumannii
Staphylococcus aureus* Poliovirus 1LSc-2ab* Enterococcusfaecium VRE
Bacillus Subtilis* Aspergillus niger* Salmonella thyphimurium
Escherichia coli* Adénovirus 5* Listeria monocytogenes
Enterococcushirae* Staphylococcs aureus MRSA
Klebsiellapneumoniae
Clostridium difficile

* full families of viruses

Purespace® Effective against the viruses

Staphylococcus aureus MRSA H1N1
Pseudomonas aeruginosa Acinétobacter H5N1
Mycobacterium smegmatis Mycobacterium tuberculosis Clostridium Difficile souche 027
Candida albicans Aspergillus niger Legionella pneumophila
Bacillus subtilis Adénovirus humain Orthopox virus
Entérovirus Polio 1

Our Certifications

The solution is certified as:
  • Medical Device Class IIA (EU Directive 93/42/CE)
The AETHER Solution is produce on the application of:
  • the European Law CE ISO 13485:2003
  • the European Law CE ISO 9001
The AETHER concept is produced and manufactured on the application of:
  • the European Law CE ISO 9001/13485 standards.
Full spectrum of activity (bactericide, virucide, sporicide and fungicide) according to a protocol issued under the:
  • NF T 72 281 (May 2009)
  • NF EN 1040
  • NF EN 1275
  • NF EN 1276
  • NF EN 1650
  • NF T 72 180
View Certifications