STN EN 17122+A1
| Name: | STN EN 17122+A1 |
| Validity: | Valid |
| Number of pages: | 40 |
| Language: |
EN
|
| Paper: | 18,90€ |
| Electronic version |
a) Only read (without ability to print and copy)
17,01€ b) Without ability to print, with ability to copy (printscreen) 18,90€ c) With ability to print and copy (printscreen) 24,57€ |
| Slovak title | Chemické dezinfekčné a antiseptické prípravky. Kvantitatívna skúška na neporéznom povrchu na vyhodnotenie virulocídnej aktivity chemických dezinfekčných a antiseptických prípravkov používaných vo veterinárnej oblasti. Skúšobné metódy a požiadavky. Fáza 2, krok 2 |
| English title | Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements - Phase2, step2 |
| Release Date: | 01. 05. 2025 |
| Date of withdrawal: | |
| ICS: | 11.080.20 |
| Sorting character/National clasification code | 85 7049 |
| Level of incorporation: | idt EN 17122:2019+A1:2024 |
| Official Journal | 04/25 |
| Amendments | |
| Replaced by: | |
| Repleces: | STN EN 17122:2020-03 (85 7049) |
| Note in Official Journal: | |
| Subject of the standard: | This European Standard specifies a test method and the minimum requirements for virucidal activity of chemical disinfectant and antiseptic products that form a homogeneous physically stable preparation when diluted with hard water, or - in the case of ready-to-use-products - with water. This European Standard applies to products that are used in the veterinary area on non-porous surfaces without mechanical action i.e. in the breeding, husbandry, production, veterinary care facilities, transport and disposal of all animals except when in the food chain following death and entry to the processing industry. EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations". NOTE 1 The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used. NOTE 2 This method corresponds to a Phase 2 Step 2 test. NOTE 3 Using this European Standard, it is possible to determine the ... |
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