AIRWALL MED

Info Request
Description:

The main characteristic of AIRWALL MED is the modern and balanced shape. It is composed by an extruded aluminium frontal profile and a steel central profile and, in order to facilitate the maintenance, it has also an upper covering easily removable. 
AIRWALL MED may have a pull switch to control the direct light and a micro-switch on the upper side of the device to control the night light. Moreover, on the lateral side a double module is dedicated to eventual additional electrical services such as the UNEL socket, general switches, etc.
AIRWALL MED is a medical device coming from I class according with the 93/42/CE directive and smi (2007/47/CE directive). According with the CEI EN 60601-1:2007+A11/2012 and UNI EN ISO 11197:2009 regulation, it is also an electromedical device from the I isolation class.


General information
  • Body: Steel structure, lateral aluminium end caps, extruded aluminium frontal profile
  • Diffuser: Glazed opal polycarbonate diffuser for indirect lighting - Opal polycarbonate diffuser for direct lighting.
  • Protection degree IP: IP20 general - IP40 lighting circuit - IP21 electrical sockets
  • Standard colour: Dry White
  • SURFACE TREATMENT ON REQUEST: Antimicrobial coating
  • STANDARD EQUIPMENT: UNEL socket 2P+T 10/16A
LIGHTING FEATURES
For version 1270 mm long
  • Indirect light: 36W - 3248lm - 4000K - CRI>90
  • Direct light: 20W - 896lm - 4000K - CRI>90
  • Night light: 3W - 155lm - 4000K - CRI>90
DIMENSIONS:
A: 245 mm
B: 770 mm - 1070 mm - 1270 mm
C: 95 mm
D: 70 mm
CLASSIFICATION ACCORDING TO THE 93/42/CEE DIRECTIVE
I class (no gas) - IIa/IIb (with gas)
- Non-stop operation
- No sections are applie
- Suitable for the installation in group 0, 1 and 2 medical premises
- Not suitable for the installation in explosion risk environments (locations with gases and flammable vapours)
- Not suitable for the installation in environments with an oxygen amount superior to the 25% with an environmental pressure until the 110kPa in usual circumstances
- Not suitable for the categories AP and APG provisions

REFERENCE DIRECTIVES AND REGULATIONS
93/42/CEE; UNI EN ISO 11197; CEI EN 60601-1; CEI EN 60598; CEI EN 55015; CEI EN 61547; UNI CEI EN ISO 14971; UNI CEI EN ISO 13485
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