DENTIRO^® Zero

Note

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  No visible surface damage or effect on the material is likely to occur when used according to label directions. No change to the integrity of the material is expected.

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  Some visible surface damage such as tarnishing or clouding may be seen with long-term exposure. Little to no effect on material intergrity is expected. Periodic wiping of surfaces with a clean damp cloth to remove residue can help to minimize damage.

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  Visible damage to the surface is likely to occur with long-term exposure and some effect on material intergrity is possible. Surfaces should be wiped with a clean damp cloth immediately after the contact time has been reached to reduce the risk of damage. Users should evaluate the risk of surface damage vs the benefits of disinfectant efficacy against pathogens to determine whether the products is appropriate for use.

The Diversity of Materials in Healthcare - From Metals and Plastics to Polymers - Makes Compatibility with Disinfectants Crucial

Recognizing and addressing material incompatibilities is crucial in the medical industry. Disinfectants that are not compatible with certain materials can trigger stress cracks in equipment, accelerating wear and tear and shortening their usable lifespan. Moreover, these cracks become breeding grounds for pathogens, rendering the disinfection processes ineffective. The longevity and functionality of medical devices hinge not just on the quality of their construction, but also on the interplay between the materials they are made of and the disinfectants used on them.

The Challenge of Environmental Stress Cracking

Environmental stress cracking presents a major issue in healthcare. When materials, notably plastics and polymers, come into contact with certain disinfectants, they can weaken and prematurely become brittle. The result is not just equipment that wears out faster but surfaces that become challenging to disinfect, turning into safe havens for pathogens.

This issue stems from the myriad of chemical structures that fall under the ❬ plastics ❭ and ❬ polymers ❭ categories. While device manufacturers choice of materials is influenced by their physical attributes, cost-effectiveness, and availability, the resilience to disinfectants is vital for patient safety.

On the other hand, disinfectants, which are made of active compounds, solvents, and other additives, need to strike a balance between eradicating microbes and not causing material damage. A lapse in this balance can lead to ❬ environmental stress cracking ❭, which weakens plastics prematurely. Prolonged exposure to certain disinfectants can alter polymer structures, making them brittle. Amines, for instance, are notably harsh on some plastics. The consequence? Deepening cracks in equipment, providing hiding spots for pathogens and undermining disinfection.

So what can be done? The remedy lies in a collaborative effort. While surface and device manufacturers should prioritize robust, durable materials, disinfectant producers must innovate with formulations that are gentler on surfaces, without compromising efficacy. At Oro Clean Chemie AG, our commitment echoes this principle, ensuring our disinfectants are both potent and compatible, so you never have to choose between clinical efficacy and equipment longevity.