TEST METHODEN 17846

Quantitative Test Method for the Evaluation of Sporicidal Activity against Clostridium difficile on Non-Porous Surfaces with Mechanical Action Employing Wipes in the Medical Area (4-Field Test)
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EN 17846 is an essential European Standard used to evaluate the sporicidal activity requirements against Clostridium difficile of wipes used in the medical area. The infographic below shows a brief insight of EN 17846.

Prior to the publication of this method, there were no standard methods available under the European Norms for Phase 2, Step 2 tests for sporicidal activity. With Clostridium difficile being a major link to healthcare-associated infections (HAIs) leading to severe symptoms such as diarrhea and colon inflammation (to name a few). This has brought attention to the importance of ensuring disinfectants used in healthcare facilities are effective in preventing the spread of this infectious disease.

Now, with the EN standard method published, chemical disinfectants can now be evaluated through the complete Phase 2 testing for its sporicidal activity against Clostridium difficile on non-porous surfaces with mechanical action.

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CUSTOMER PROCESS
Step 1: Which category does your product fall under?

These are the categories of test products tested under EN 17846:

  • Surface disinfectant
  • Ready-to-use wipes pre-soaked with surface disinfectant
Step 2: Select your test microorganisms

This test method is specially developed for Clostridium difficile.

Other bacterial spore strains may be tested including:

  • Bacillus cereus
  • Bacillus subtilis

Wish to add more microorganisms? Click here for our full list of microorganisms.

Step 3: Select an appropriate contact time and concentration for your test product

The test concentration is chosen according to the manufacturer’s recommendation.

These are the minimum contact times given by the test method:

  • Between 1 to 30 minutes for surfaces which are frequently touched by different people
  • Between 1 to 60 minutes for other surfaces
Step 4: What are the soiling conditions associated with your test product?

Interfering substances, or commonly referred to as soiling, are used to mimic organic substances found on human skin, surfaces, and instruments. These are the available soiling conditions according to the test method:

  • Clean condition: 0.3 g/L bovine serum albumin
  • Dirty condition: 3.0 g/L bovine serum albumin and 3.0 mL/L sheep erythrocytes
Step 5: What are the repetitions and precision steps in this standard method?

This test method lays out specific repetitions according to the following test schedule:

  • Test Run 1: 1 carrier, 2 concentrations/contact times
  • Test Run 2: 2 carriers, claimed concentration and contact time
Step 6: Place an order and send your sample to us

Fill the test request form and place an order via email at info@tecolab-global.com. We will advise on the quantity of sample required for testing.

You can deliver the sample to us via courier and provide us the tracking code. We will monitor the delivery status and inform you when we receive the sample.

Step 7: Track the status of your request

Once we have received your sample, we will provide a tracking number to you. You can easily track the status of your request here.

Step 8: Download your password-protected test report

Download your readily available test report online with just a single click using the link and password provided via email notification. We will receive a notification once you have downloaded the test report.

For safety purposes, the uploaded test report will self-destruct after 7 days.

Step 9: Analyze your passing criteria in the test report with our laboratory experts

In order to pass the test, the product shall demonstrate at least a 4 decimal log (lg) reduction on test field 1 and the mean number of colonies on test fields 2 to 4 shall not exceed 50.

Need assistance with your test report? Discuss your results with our microbiologists for more information.