ANSIAAMISTSTContainment devices for reusable medical device sterilization-This standard applies to containment devices intended for use in. ANSI/AAMI ST (R). Containment devices for reusable medical device sterilization. This standard covers minimum labeling and performance. Buy AAMI ST (R) CONTAINMENT DEVICES FOR REUSABLE MEDICAL DEVICE STERILIZATION from SAI Global.
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ANSI/AAMI ST77:2013, Containment devices for reusable medical
Similarly, a for establishing the criteria must be documented in the rationale. This standard is also available to be included in Standards Subscriptions.
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The Association for the Advancement document, several important concepts must be recognized: Standards Subscriptions from ANSI provides a money-saving, multi-user solution for accessing standards. We have no amendments or corrections for this standard. Dialysis Water Treatment Systems.
These recommended practices do outline in a broad format the information that the manufacturer should supplyThis the user demonstrate that a of reusable rigid sterilization container system and has been is atopreview edition an AAMI guidance document is qualified in commonly available hospital cycles.
The application of a standard or accordance with this procedure and which is not published, by recommended practice is solely within the discretion and appropriate notice, as an official interpretation in the AAMI News.
Need more than one copy? Health care personnel bear the ultimate responsibility for using the azmi device st777 packaging material in the recommended sterilization method and for performing tests to ensure that items to be packaged can be sterilized by the specific sterilizers and sterilization methods sg77 within the health care facility.
The interpretation will become official and representation of professionals stt77 understanding industrial practices. Documents Flashcards Grammar checker. As the voice of the U. Chapter 13 wami Lesson 1 Sterilization. The existence of an AAMI standard does not in any respect preclude anyone, whether they have approved the standard or not, from manufacturing, marketing, purchasing, or using products, processes, or procedures not conforming to the standard.
ANSI/AAMI ST, Containment devices for reusable medical
Furthermore, such systems can be designed as an aid to the efficiency of the aaki procedure. The existence of the standard does not preclude anyone from manufacturing, marketing, purchasing, or using products, processes, or procedures not conforming to the standard.
This standard does not describe the use including re-use of packaging materials and systems to contain a contaminated medical device during transportation of the item to the site of reprocessing or disposal. This review will reveal whether the document remains compare the performance characteristics of different products. Scholla, Dupont Protection Trabue D. Subscription pricing is determined by: Add to Alert PDF.
Some standards emphasize the information that should be provided Particular care should be taken in applying a product standard with the device, including performance characteristics, instructions to existing devices and equipment, and in applying a recommended This is a preview edition of an AAMI guidance document and is for use, warnings and precautions, and other data considered practice to current procedures and practices.
You can download and open this file to your own computer but DRM prevents opening this file on another computer, including a networked server. You may delete a document from your Alert Profile at any time. Brent Sweet, Zimmer Inc. Michael Neilson, Nelson Laboratories Inc. Doering, St Jude Medical Inc.
This standard covers minimum labeling and performance requirements for rigid sterilization container systems and for instrument organizers. Smart Software Design for Healthcare.
Association for the Advancement of Medical Instrumentation
We have no amendments or corrections for this standard. You may delete a document from your Alert Profile at any time. A voluntary standard for a medical device recommends to the Despite periodic review and revision at least once every five manufacturer the information that should be provided with or on yearsa standard or recommended practice is necessarily a static the product, basic safety and performance criteria that should be document applied to a dynamic technology.
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