EN 17422 Veterinary Teat Disinfectant Test (Phase 2 Step 2)

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Summary

EN 17422 is a Phase 2, Step 2 quantitative surface test that assesses the bactericidal efficacy of veterinary teat disinfectants applied pre and post milking. The standard simulates real-use conditions on synthetic skin surfaces, including defined soiling to measure microbial reduction without mechanical action, ensuring disinfectants meet performance requirements for mastitis prevention.

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Quick understanding of the test

EN 17422:2022 - Quantitative surface test method for the evaluation of teat disinfectants used in the veterinary area (phase 2 step 2)

EN 17422 (phase 2 step 2) evaluates the bactericidal activity of teat disinfectants used in the veterinary area.

Application

Applicable for disinfectants used on teat skin as a pre/post-milking treatment in veterinary settings.
  • A bacterial suspension mixed with an interfering substance is applied to synthetic skin test surfaces and held for a specific period of conditioning.
  • Afterward, the test surface is immersed in a disinfectant solution for a specified duration, followed by neutralization, plating, and incubation.
  • Post incubation, bacteria are enumerated and reduction rate is determined.

Turnaround Time

It typically takes 3-4 weeks.
Results are evaluated by measuring the reduction in viable microorganisms on treated surfaces compared to untreated controls.

Passing criteria

A product must demonstrate a 3-log reduction for pre-milking teat disinfectants and 4-log reduction for post-milking teat disinfectants.

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What Is EN 17422 Test?

EN 17422 is designed to evaluate the bactericidal activity of pre/post – milking teat disinfectants disinfectants applied on the teat skin without mechanical action  EN 17422 is a quantitative carrier based test (phase 2, step 2) that uses synthetic test surfaces along with other conditions to replicate real-world product usage scenarios within a controlled laboratory setting.

 EN 17422 helps demonstrate that teat disinfectants meet required performance criteria to support mastitis prevention claims required under EU veterinary hygiene and biocidal product frameworks.

Veterinary Applications of EN 17422

This test is designed for pre- and post-milking teat disinfectants used in 

  • Breeding, 
  • Husbandry, 
  • Production, 
  • Transport, 
  • Veterinary care, and 
  • Disposal of animals (excluding food chain processing).

EN 17422 Test Conditions & Requirements

Parameter

SIST EN 17422

SIST EN 1656

Purpose

Quantitative surface test to evaluate teat disinfectants used in the veterinary area (Phase 2, Step 2)

Quantitative suspension test to evaluate bactericidal activity of chemical disinfectants/antiseptics used in the veterinary area (Phase 2, Step 1)

Scope of products

Only teat disinfectants used on teat skin without mechanical action (pre- and/or post-milking)

Veterinary disinfectants for equipment (immersion), surface disinfection (wiping/spraying/flooding), and teat disinfection

log reduction 

Post-milking –  ≥ 4 log reduction Pre-milking –  ≥ 3 log reduction 

≥ 5 log reduction 

Interfering substances 

Post-milking – milk powder (final 10 g/L)

Pre-milking – bovine albumin (final 3 g/L)

For teat disinfectants –

Post milking: 10,0 g/l of milk powder

Pre-milking: 3,0 g/l bovine albumin

For other disinfection purposes – 

3,0 g/l bovine albumin(low soiling), 10 g/l yeast extract + 10 g/l bovine albumin (High soiling)


Mandatory Test organisms 


Escherichia coli (ATCC 8739) , Staphylococcus aureus (ATCC 6538P)

General veterinary disinfectants: Enterococcus hirae, Proteus hauseri, Pseudomonas aeruginosa, Staphylococcus aureus
Teat disinfectants: Escherichia coli, Staphylococcus aureus, Streptococcus uberis

EN 17422 Test Method Overview

  • Bacterial test suspension with interfering substance is inoculated onto a synthetic skin test surface and held at 30 °C for a specific period of conditioning.
  • Following the conditioning time, inoculated test surface is immersed in the  disinfectant samples / dilutions of the product for a specific contact time.
  •  At the end of that contact time, test surface is transferred into the neutralizer.
  • The bacteria are removed from the test surface by ultrasound technique. Bacteria recovered in neutralizing solution are enumerated by plate count method. 
  • The  number of surviving bacteria recovered from the treated surface is compared with the number of bacteria observed in the control test. (In  control test, surface is exposed to water instead of the disinfectant product)

Note – Pre-milking teat disinfectants are evaluated under clean conditions, focusing on rapid bacterial reduction to minimize contamination risk prior to milk collection. In contrast, post-milking teat disinfectants are tested under soiled conditions, simulating exposure to milk residues and organic matter to verify bactericidal activity after milking.

By incorporating these differentiated conditions, EN 17422 ensures that efficacy data accurately reflects real-world application and meets European regulatory requirements for veterinary teat disinfectant products.

Interpretation of EN 17422 Test Results

As per EN 17422 passing criteria, the test product is evaluated against control samples.

  • Post-milking disinfectants must demonstrate a minimum 4-log reduction
  • Pre-milking disinfectants must demonstrate a minimum 3-log₁₀  reduction 

EN 17422 vs Other Veterinary Teat Disinfectant Tests

Parameter

SIST EN 17422

SIST EN 1656

Purpose

Quantitative surface test to evaluate teat disinfectants used in the veterinary area (Phase 2, Step 2)

Quantitative suspension test to evaluate bactericidal activity of chemical disinfectants/antiseptics used in the veterinary area (Phase 2, Step 1)

Scope of products

Only teat disinfectants used on teat skin without mechanical action (pre- and/or post-milking)

Veterinary disinfectants for equipment (immersion), surface disinfection (wiping/spraying/flooding), and teat disinfection

log reduction 

Post-milking –  ≥ 4 log reduction Pre-milking –  ≥ 3 log reduction 

≥ 5 log reduction 

Interfering substances 

Post-milking – milk powder (final 10 g/L)

Pre-milking – bovine albumin (final 3 g/L)

For teat disinfectants –

Post milking: 10,0 g/l of milk powder

Pre-milking: 3,0 g/l bovine

albumin

For other disinfection purposes – 

3,0 g/l bovine albumin

10 g/l yeast extract

plus 10 g/l bovine

albumin


Mandatory Test organisms 


Escherichia coli (ATCC 8739) 

Staphylococcus aureus (ATCC 6538P)

General veterinary disinfectants: Enterococcus hirae, Proteus hauseri, Pseudomonas aeruginosa, Staphylococcus aureus
Teat disinfectants: Escherichia coli, Staphylococcus aureus, Streptococcus uberis

Importance of EN 17422 Test

In veterinary settings, teat disinfection before and after milking is a vital practice to reduce the number of pathogens causing mastitis. Mastitis is an inflammation of the mammary gland and is predominantly caused by bacterial pathogens and occasionally mycotic or algal microbes. Mastitis infection is a common concern among dairy animals which results in substantial economic losses within the dairy sector.

EN 17422 test is an important and widely accepted industry standard that helps to verify the claims of disinfectant products specifically formulated for teat disinfection in veterinary applications. By complying with EN 17422, manufacturers and dairy producers can be confident that teat disinfectants meet stringent performance criteria. This helps to safeguard animal health by minimizing the spread of mastitis-causing pathogens and ensures that products deliver reliable antimicrobial action without relying on mechanical cleaning action.

Why Choose Our Lab for EN 17422 Testing

At MIS, we provide accurate EN 17422 testing to evaluate the bactericidal performance of teat disinfectants under real-world veterinary conditions.

Our experts tailor testing studies as per product’s intended use to ensure results are reliable and accurate.

We support you from study planning through final reporting, helping you generate high-quality data to validate formulations, support  compliance needs, and confidently support your EN 17422 product claims.

Request EN 17422 Testing

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Frequently Asked Questions

DR. Martinoz Scholtz

MIS Labs
1. What is EN 17422 testing used for?

EN 17422 evaluates the bactericidal efficacy of pre-milking and post-milking veterinary teat disinfectants under practical, real-world conditions using a carrier test on synthetic skin.

2. Is EN 17422 required for teat disinfectants?

Yes.  It is typically required to support regulatory approval and product claims under the EU Biocidal Products Regulation (BPR) for teat disinfection use.

3. What is the difference between EN 17422 and EN 1656?

EN 1656 is a suspension test (Phase 2, Step 1) that evaluates bactericidal activity in a liquid medium, while EN 17422 is a surface/carrier test (Phase 2, Step 2) using synthetic skin to simulate real teat application, simulating more real conditions.

4. What log reduction is required under EN 17422?

EN 17422 requires a minimum ≥ 3 log₁₀ reduction for pre-milking teat disinfectants and ≥ 4 log₁₀ reduction for post-milking teat disinfectants. 

5. Which products need EN 17422 testing?

EN 17422 applies to pre- and post-milking teat disinfectants intended for use on teat skin in veterinary settings without mechanical action.

6. How long does EN 17422 testing take?

EN 17422 typically takes 3-4 weeks to complete.

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