STERISEPT PLUS is suitable for use in hospitals, the food and pharmaceutical industries, veterinary practices, laboratories, dental clinics, and other healthcare institutions.
The product has broad bactericidal (including against the tuberculosis-causing agent), sporicidal, virucidal, and fungicidal effects, destroying Gram-negative and Gram-positive bacteria, including the tuberculosis-causing agent, fungi, and deactivating both enveloped and non-enveloped viruses (including HBV, HIV, rotavirus, and adenovirus).
Usage:
STERISEPT PLUS is a concentrate. Dilute according to the required effectiveness (see microbiology).
To prepare the working solution, dilute the product with water at room temperature. Apply the working solution to the surface using a cloth or towel, ensuring the surface is thoroughly covered. Recommended contact time is 15 minutes.
Treated surfaces do not need to be rinsed (except for food-contact surfaces).
The mixed working solution is usable for up to 30 days. Store in an airtight container at room temperature. The product is suitable for use on stainless steel, glass, aluminum, copper, brass, and ceramic surfaces, as well as linoleum, PVC, rubber, plastic, and silicone surfaces.
It is not suitable for use on polycarbonate and lacquered surfaces.
The concentration of quaternary ammonium compounds in the working solution of Sterisept Plus is less than 0.5%.
Precautions:
Harmful if swallowed. Toxic to aquatic organisms with long-term effects. Causes severe skin burns and eye damage. May cause organ damage with prolonged or repeated exposure (oral) and may cause respiratory irritation. Do not inhale vapors, avoid release into the environment. Wear protective gloves, protective clothing, eye protection, and a face mask.
If swallowed: rinse mouth. DO NOT induce vomiting.
If on skin (or hair): immediately remove contaminated clothing. Rinse skin with water or shower.
If in eyes: rinse carefully with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Immediately contact a POISON CENTER or doctor.
Dispose of contents/container according to hazardous waste or packaging waste regulations.
Composition:
100 g of the product contains active substances: Didecyl-Dimethyl-Ammonium Chloride (DDAC) 12.5 g; N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine 12.5 g.
Registered with the Medicines Agency’s Department of Medical Devices.
Has CE marking according to the Medical Devices Directive.