以專利技術研製,自身免疫系統中的次氯酸,造成真正天然的配方,對身體和環境都無毒及無害,且不會造成刺激。
- 天然安全,動物舔食無需顧慮,對身體和環境無害。
- 不含酒精、抗生素、類固醇。
- 家居清潔。
- 淨化室內空氣。
- 健康維護。
以專利技術研製,自身免疫系統中的次氯酸,造成真正天然的配方,對身體和環境都無毒及無害,且不會造成刺激。
- 天然安全,動物舔食無需顧慮,對身體和環境無害。
- 不含酒精、抗生素、類固醇。
電解水(99.962%),氯化鈉(0.023%)輔助物質:次氯酸鈉(0.0020%)、次氯酸(0.0130%)
麥高辰淨化抗菌劑是全球少數能同時得到4樣EN 測試報告(EN1276、EN1650、EN14476、EN13704)。
安全如水,對人體完全無害。
如要居家環境抗菌,一定要選用有經過測試檢驗的,才有保障。
EN 1276 QUANTITATIVE SUSPENSION TEST OF BACTERICIDAL ACTIVITY OF CHEMICAL DISINFECTANTS
Summary of Test
The EN method below are designed to evaluate the bactericidal, fungicidal, yeasticidal, basic sporicidal or mycobactericidal activity of a product used under various conditions. Many methods are suspension based and are used to support general antimicrobial claims while other test methods are carrier-based and are used to support antimicrobial activity of products on surfaces or devices. In either case, the same general principles apply. The test organism is exposed to sample of the product in a manner which simulates the desired claim. Following exposure, the test system is neutralized and quantitatively assayed for survivors. The resulting plates are incubated, enumerated, and a reduction in viability or microbiocidal effect is determined as compared to a population control.
Test Organisms |
Staphylococcus aureus, Pseudomonas aeruginosa, Enterococcus hirae, Escherichia coli |
Purpose of Test |
Suspension-based study formally used to evaluate bactericidal activity. |
Typical Performance Criteria (Requirements may vary by claim) |
5 log reduction in ≤5 minutes |
EN 1650 QUANTITATIVE SUSPENSION TEST FOR THE EVALUATION OF FUNGICIDAL ACTIVITY OF CHEMICAL DISINFECTANTS
Summary of Test
The EN method below are designed to evaluate the bactericidal, fungicidal, yeasticidal, basic sporicidal or mycobactericidal activity of a product used under various conditions. Many methods are suspension based and are used to support general antimicrobial claims while other test methods are carrier-based and are used to support antimicrobial activity of products on surfaces or devices. In either case, the same general principles apply. The test organism is exposed to sample of the product in a manner which simulates the desired claim. Following exposure, the test system is neutralized and quantitatively assayed for survivors. The resulting plates are incubated, enumerated, and a reduction in viability or microbiocidal effect is determined as compared to a population control.
Test Organisms |
Candida albicans, Aspergillus brasiliensis |
Purpose of Test |
Suspension-based study formally used to evaluate fungicidal activity. |
Typical Performance Criteria |
4 log reduction in ≤15 minutes |
EN 14476 QUANTITATIVE SUSPENSION TEST FOR THE EVALUATION OF VIRUCIDAL ACTIVITY OF CHEMICAL DISINFECTANTS AND ANTISEPTICS IN HUMAN MEDICINE
Purpose of Test
The purpose of this test is to determine the minimum virucidal activity of a chemical disinfectant in contact with medical instruments, surfaces or hands, according to EN test methods developed by the CEN (European Committee for Standardization) to support registrations within Europe. The method described is intended to determine the activity of chemical disinfectants that form a homogeneous, physically stable preparation in hard water – or in the case of ready-to-use products – with deionized water, and in the conditions in which they are used.
Summary of Test
A suspension of virus is added to a solution of interfering substances; the interfering substance used is dependent on the product claim. The prepared test product is added to the suspension of virus in interfering substance and is maintained at the requested temperature for the requested exposure time(s). At the end of the exposure time, aliquots are taken and the virucidal activity against the test virus is immediately neutralized or suppressed by dilution in ice-cold test medium. Serial dilutions are performed and the dilutions are then assayed for viral infectivity by an assay method specific for the testing virus. Appropriate controls are performed in parallel with the assay. Reduction of virus infectivity is calculated from differences of log virus titers before and after treatment with the product.
Test Organisms |
Adenovirus, Poliovirus Bovine, Parvovirus, and additional pathogens |
Purpose of Test |
Suspension-based study used as a presumptive test to evaluate virucidal activity. |
Typical Performance Criteria |
4 log reduction |
EN 13704 QUANTITATIVE SUSPENSION TEST FOR THE EVALUATION OF SPORICIDAL ACTIVITY OF CHEMICAL DESINFECTANTS USED IN FOOD, INDUSTRIAL, DOMESTIC AND INSTITUTIONAL AREAS
Purpose of test
Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants used in food, industrial, domestic and institutional areas. Not suited in situations where disinfection is medically indicated or when products are used on living tissues with the exception for hand hygiene in the above instances.
Products that can be tested
Chemical disinfectant products that form homogenous, physically stable preparations in hard water for use in the above instances.
Description of Test
· A test suspension of Bacillus subtilis spores in a solution of interfering substance, simulating clean conditions, is added to a prepared sample of the product under test diluted in hard water.
· The mixture is maintained at 20°C ± 1°C for 60 minutes ± 10 seconds.
· At the end of the contact time, a portion is taken and the sporicidal action in this portion is immediatedly neutralized or suppressed by a validated method.
The number of surviving bacterial spores in each sample are determined. The reduction in viable counts is calculated.
生產地:墨西哥。
34oz (1L)