STN EN 1657
| Name: | STN EN 1657 |
| Validity: | Valid |
| Number of pages: | 52 |
| Language: |
EN
|
| Paper: | 21,40€ |
| Electronic version |
a) Only read (without ability to print and copy)
19,26€ b) Without ability to print, with ability to copy (printscreen) 21,40€ c) With ability to print and copy (printscreen) 27,82€ |
| Slovak title | Chemické dezinfekčné a antiseptické prípravky. Kvantitatívna suspenzná skúška na vyhodnotenie základnej fungicídnej alebo kvasinkocídnej aktivity chemických dezinfekčných a antiseptických prípravkov používaných vo veterinárstve. Skúšobná metóda a požiadavky (fáza 2, krok 1) |
| English title | Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1) |
| Release Date: | 01. 05. 2025 |
| Date of withdrawal: | |
| ICS: | 71.100.35 |
| Sorting character/National clasification code | 85 7058 |
| Level of incorporation: | idt EN 1657:2024 |
| Official Journal | 04/25 |
| Amendments | |
| Replaced by: | |
| Repleces: | STN EN 1657:2016-10 (80 7033) |
| Note in Official Journal: | |
| Subject of the standard: | This document specifies a test method and the minimum requirements for fungicidal or yeasticidal 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. Products can only be tested at a concentration of 80 % or less, as some dilution is always produced by adding the test organisms and interfering substance. This document applies to products that are used in the veterinary area - 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 into processing industry. This document also applies to products used for teat disinfection. 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 ... |
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