{"id":457387,"date":"2024-10-20T09:50:53","date_gmt":"2024-10-20T09:50:53","guid":{"rendered":"https:\/\/pdfstandards.shop\/product\/uncategorized\/aami-tir99-2024\/"},"modified":"2024-10-26T18:17:57","modified_gmt":"2024-10-26T18:17:57","slug":"aami-tir99-2024","status":"publish","type":"product","link":"https:\/\/pdfstandards.shop\/product\/publishers\/aami\/aami-tir99-2024\/","title":{"rendered":"AAMI TIR99 2024"},"content":{"rendered":"

Provides guidance for the proper processing of dilators and ultrasound probes in health care facilities to assist in making them safe and effective for use in patient care. Includes the information on selection and use of cleaning, disinfection and sterilization systems that have been cleared for marketing by the FDA for use in hospitals and other health care facilities.<\/p>\n

PDF Catalog<\/h4>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
PDF Pages<\/th>\nPDF Title<\/th>\n<\/tr>\n
1<\/td>\nAAMI TIR99:2024; Processing of dilators, transesophageal and ultrasound probes in health care facilities <\/td>\n<\/tr>\n
3<\/td>\nTitle page <\/td>\n<\/tr>\n
4<\/td>\nAAMI Technical Information Report
Copyright information <\/td>\n<\/tr>\n
5<\/td>\nContents <\/td>\n<\/tr>\n
6<\/td>\nCommittee representation <\/td>\n<\/tr>\n
12<\/td>\nForeword <\/td>\n<\/tr>\n
13<\/td>\n1 Scope
1.1 General
1.2 Inclusions <\/td>\n<\/tr>\n
14<\/td>\n1.3 Exclusions
2 Normative references
3 Terms and definitions <\/td>\n<\/tr>\n
19<\/td>\n4 Information to be provided to users by the reusable device manufacturer
4.1 Labeling of reusable devices, including processing validation <\/td>\n<\/tr>\n
20<\/td>\n5 Assigning Spaulding classification
5.1 General <\/td>\n<\/tr>\n
21<\/td>\n5.2 Application to dilators and ultrasound probes
5.2.1 Critical devices (Table 1 and Sect. 5.1)
5.2.2 Risk assessment
Table 1\u2014Spaulding classification applied to example ultrasound procedures and dilator use <\/td>\n<\/tr>\n
22<\/td>\n5.3 Integrating decision-making about Spaulding classification with clinical workflow
6 Use of probe covers <\/td>\n<\/tr>\n
23<\/td>\n7 Use of ultrasound gel and accessories
7.1 Ultrasound transmission gel (USTG)
7.2 Accessories
7.2.1 Needle guides
7.2.2 Bite guards
7.2.3 Dilator guidewires
8 Design of processing area <\/td>\n<\/tr>\n
25<\/td>\n9 Personnel education, training and competency
9.1 Personal protective equipment <\/td>\n<\/tr>\n
26<\/td>\n10 Cleaning
10.1 General considerations
10.2 Point of use treatment <\/td>\n<\/tr>\n
27<\/td>\n10.3 Containment and transport of contaminated devices
10.3.1 Containment of contaminated items for transport to the decontamination area
10.3.2 External transport of contaminated devices <\/td>\n<\/tr>\n
28<\/td>\n10.4 Electrical leak testing
10.5 Manual and mechanical cleaning <\/td>\n<\/tr>\n
29<\/td>\n10.6 Rinsing and drying
10.7 Inspection <\/td>\n<\/tr>\n
30<\/td>\n10.7.1 Cleaning verification
11 Disinfection
11.1 General considerations
11.2 Low-level disinfection and intermediate-level disinfection <\/td>\n<\/tr>\n
31<\/td>\n11.3 High-level disinfection
11.3.1 Liquid chemical sterilants (LCSs) and high-level disinfectants (HLDs) <\/td>\n<\/tr>\n
32<\/td>\n11.3.2 High-level disinfection methodologies
11.3.2.1 Automated\/mechanical disinfection process
11.3.2.2 Manual high-level disinfection <\/td>\n<\/tr>\n
33<\/td>\n11.4 Cycle verification
11.5 Drying after high-level disinfection
12 Sterilization
12.1 General
12.2 Types of sterilization processes <\/td>\n<\/tr>\n
34<\/td>\n12.3 Sterilization packaging
12.4 Cycle verification for sterilization <\/td>\n<\/tr>\n
35<\/td>\n13 Transport of high-level disinfected and sterile items
14 Storage <\/td>\n<\/tr>\n
36<\/td>\n14.1 TEE probes <\/td>\n<\/tr>\n
37<\/td>\n14.2 Storage duration
15 Documentation and traceability <\/td>\n<\/tr>\n
38<\/td>\n16 Quality control
16.1 General criteria
16.2 Quality process improvement
Table 2\u2014Continuous quality improvement matrix <\/td>\n<\/tr>\n
39<\/td>\n16.3 Risk analysis
Table 3\u2014Example risk assessment matrix <\/td>\n<\/tr>\n
41<\/td>\nTable 4\u2014Algorithm for suggested workflow for transrectal, transvaginal & surface ultrasound device point of use processing <\/td>\n<\/tr>\n
42<\/td>\n16.4 Policies and procedures <\/td>\n<\/tr>\n
43<\/td>\n16.5 Product recalls <\/td>\n<\/tr>\n
44<\/td>\nAnnex A (informative) Literature and Studies for Probe Use and Processing <\/td>\n<\/tr>\n
47<\/td>\nAnnex B (informative) Supplementary Information <\/td>\n<\/tr>\n
49<\/td>\nBibliography <\/td>\n<\/tr>\n<\/table>\n","protected":false},"excerpt":{"rendered":"

AAMI TIR99:2024 Processing of dilators, transesophageal and ultrasound probes in health care facilities<\/b><\/p>\n\n\n\n\n
Published By<\/td>\nPublication Date<\/td>\nNumber of Pages<\/td>\n<\/tr>\n
AAMI<\/b><\/a><\/td>\n2024<\/td>\n53<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"featured_media":457394,"template":"","meta":{"rank_math_lock_modified_date":false,"ep_exclude_from_search":false},"product_cat":[2654],"product_tag":[],"class_list":{"0":"post-457387","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-aami","8":"first","9":"instock","10":"sold-individually","11":"shipping-taxable","12":"purchasable","13":"product-type-simple"},"_links":{"self":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product\/457387","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/types\/product"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media\/457394"}],"wp:attachment":[{"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/media?parent=457387"}],"wp:term":[{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_cat?post=457387"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/pdfstandards.shop\/wp-json\/wp\/v2\/product_tag?post=457387"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}