Whiteley Aidal Plus Information
Aidal Plus is a stable, odour suppressed, mildly acidic 2% glutaraldehyde based sterilant.
# | Attribute | Value |
---|---|---|
1. | Function | Disinfectant Solution |
2. | Pack Size | 5 Litre Bottle |
3. | Supplier Code | 10082 |
4. | Pack Type | Bottle |
5. | Contents | 5 Litre Bottle |
6. | brand | WHITELEY |
Aidal® Plus is a stable, odour suppressed, mildly acidic 2% glutaraldehyde based sterilant suitable for use in hospitals, dental/medical surgeries and veterinary hospitals. It is used for the sterilisation and high level disinfection of critical and semi critical medical devices.
AIDAL® PLUS is suitable for use in hospitals, dental and medical surgeries and veterinary hospitals, for the sterilisation and high level disinfection of critical and semi critical medical devices.
AIDAL® PLUS is a polyglycol dialdehyde complex instrument disinfectant intended for general use in a surgical practice where sterilisation or high level disinfection is required. It is a stable, odour suppressed, mildly acidic glutaraldehyde sterilant and instrument disinfectant (high level), which exhibits potent biocidal action.
AIDAL® PLUS shows several major improvements over alkaline activated glutaraldehyde. Improved biocidal performance is achieved with reduced glutaraldehyde odour and reduced propensity for irritation and yellowing to human skin compared with alkaline glutaraldehyde preparations.
AIDAL® PLUS has been tested in a wide array of tests and various conditions, including testing at the end of the shelf life, at the end of the re-use period, diluted to the minimum recommended concentration of active material (1.5% Glutaraldehyde), and then soiled and tested in hard water against hardest to kill organisms.
AIDAL® PLUS will not damage endoscopes or other complex medical equipment when used in accordance with directions and the instrument manufacturers instructions.
AIDAL® PLUS has an MRC (minimum recommended concentration) of 1.5% w/w glutaraldehyde. All tests for sterilant or disinfectant efficacy were conducted at the MRC or lower in accordance with strict performance standards.