{"id":279451,"date":"2024-10-19T18:51:37","date_gmt":"2024-10-19T18:51:37","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/bsi-14-30300957-dc\/"},"modified":"2024-10-25T15:25:32","modified_gmt":"2024-10-25T15:25:32","slug":"bsi-14-30300957-dc","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/bsi\/bsi-14-30300957-dc\/","title":{"rendered":"BSI 14\/30300957 DC"},"content":{"rendered":"
PDF Pages<\/th>\n | PDF Title<\/th>\n<\/tr>\n | ||||||
---|---|---|---|---|---|---|---|
1<\/td>\n | 30300957 <\/td>\n<\/tr>\n | ||||||
8<\/td>\n | 41_e_stf 1 Scope 2 Normative references 3 Terms and definitions <\/td>\n<\/tr>\n | ||||||
9<\/td>\n | 4 Classification 5 Requirements 5.1 Microbicidal dressings 5.2 Microbistatic dressings 5.3 Performance Table 6 Information to be supplied <\/td>\n<\/tr>\n | ||||||
11<\/td>\n | Annex A (normative) Validation of dilution-neutralisation A.1 Principle A.2 Neutralizer selection A.3 Preparation of microbial suspension A.4 Test validation <\/td>\n<\/tr>\n | ||||||
12<\/td>\n | A.5 Neutralizer toxicity <\/td>\n<\/tr>\n | ||||||
13<\/td>\n | A.6 Test organism viability A.7 Neutralisation Effectiveness <\/td>\n<\/tr>\n | ||||||
14<\/td>\n | A.8 Interpretation of data <\/td>\n<\/tr>\n | ||||||
15<\/td>\n | Annex B (informative) Neutralizers <\/td>\n<\/tr>\n | ||||||
16<\/td>\n | Annex C (informative) Rationale C.1 Title C.2 Microbial strains <\/td>\n<\/tr>\n | ||||||
17<\/td>\n | C.3 Cutting dressings C.4 Positive control C.5 Microbistatic requirements C.6 Performance Requirements C.7 Test method Information C.7.1 General <\/td>\n<\/tr>\n | ||||||
18<\/td>\n | C.7.2 Direct Contact method C.7.3 Shaking Method C.7.4 Two compartment method C.8 Media C.9 Incubation Temperatures C.10 Dressing Classification <\/td>\n<\/tr>\n | ||||||
19<\/td>\n | Annex D (informative) Apparatus <\/td>\n<\/tr>\n | ||||||
20<\/td>\n | Annex E (informative) Reagents and culture media E.1 General E.2 Water E.3 Tryptone Soya Agar E.4 Maximum recovery diluent E.5 Simulated Wound Fluid (SWF) <\/td>\n<\/tr>\n | ||||||
21<\/td>\n | E.6 Sabouraud agar (SAB) E.7 Neutralizer <\/td>\n<\/tr>\n | ||||||
22<\/td>\n | Annex F (informative) Reference strains F.1 Storage of strains F.2 Bacterial strains F.3 Yeasts and molds F.4 Other Strains <\/td>\n<\/tr>\n | ||||||
23<\/td>\n | Annex G (informative) Preparation of microbial suspensions G.1 Stock Cultures G.2 Working Culture G.2.1 Subcultures from stocks G.2.2 Preparation of suspensions on day of testing <\/td>\n<\/tr>\n | ||||||
24<\/td>\n | Annex H (normative) Test methods H.1 Introduction H.2 Equilibration of reagents H.3 Neutralizer H.4 Choice of experimental conditions H.4.1 Contact Times H.4.2 Strains <\/td>\n<\/tr>\n | ||||||
25<\/td>\n | H.4.3 Saturation Volume H.5 Sample Size H.6 Direct contact test method H.6.1 Microbial Suspension H.6.2 Preparation of test samples H.6.3 Exposing the dressings to test organisms <\/td>\n<\/tr>\n | ||||||
26<\/td>\n | H.7 Shaking method H.7.1 Sampling Volume H.7.2 Microbial Test Suspension H.7.3 Preparation of test samples <\/td>\n<\/tr>\n | ||||||
27<\/td>\n | H.7.4 Exposing the test samples to the test organisms H.8 Two compartment method H.8.1 Microbial Test Suspension H.8.2 Preparation of test samples H.8.3 Exposing the test samples to the test organisms <\/td>\n<\/tr>\n | ||||||
28<\/td>\n | H.9 Recovery and enumeration of test organisms H. 10 Calculation and expression of results H.10.1 Calculation of Viable counts (cfu\/ml) <\/td>\n<\/tr>\n | ||||||
29<\/td>\n | H.10.2 Calculation of viable counts per sample H.10.3 Judgement of test validity <\/td>\n<\/tr>\n | ||||||
30<\/td>\n | H.10.4 Calculation of the detection limit of the test H.10.5 Calculation of antimicrobial activity <\/td>\n<\/tr>\n | ||||||
31<\/td>\n | H.11 Test report <\/td>\n<\/tr>\n | ||||||
32<\/td>\n | Annex I (informative) Figures and illustrations <\/td>\n<\/tr>\n | ||||||
34<\/td>\n | Annex ZA (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 93\/92\/EEC on medical devices <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":" BS EN 16756. Antimicrobial wound dressings. Requirements and test methods<\/b><\/p>\n |