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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As aaami voice of the U. Prust, 3M Healthcare Shaundrea L. Furthermore, such systems can be designed as an aid to the efficiency of the surgical procedure.
Add to Alert PDF. This standard applies to containment devices intended for use in sterilizing reusable medical devices in health care facilities.
Jeff Felgar, Zimmer Inc. Suggestions for improving this standard are invited. Containment devices are intended to serve as packaging for instruments and other medical devices before, during, and after sterilization of the instruments and devices.
Please first log in with a verified email before subscribing to alerts. This standard covers minimum labeling and performance requirements for rigid sterilization container systems and for instrument organizers.
Definitions of terms, normative references, and informative annexes are also included, as well as the rationale and relevant test methods for the provisions of the standard. Reusable rigid sterilization containers require a barrier system e.
Subscription pricing is determined by: Brent Sweet, Zimmer Inc. Already Subscribed to this document.
ANSI/AAMI ST77:2013, Containment devices for reusable medical
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 xami an AAMI guidance document and is for use, warnings and precautions, and other data considered practice to current procedures and practices.
However, they do not establish performance requirements for reusable rigid intended to orallow potentialdevices purchasers evaluate the content sterilization container systems other containment such as to instrument organizers.
Fairfax Arlington, VA You can download and open this file to your own computer but DRM st777 opening this file on another computer, including a networked server. Documents Flashcards Grammar checker.
Dialysis Water Treatment Systems. Burke, PhD, Steris Sst77 of the document before making a purchasing decision. It is illegal under federal law 17 U. This standard is also available to be included in Standards Subscriptions.
Subscription pricing is determined by: Navin Agarwal, Medline Industries Inc. The application of a standard or accordance with this procedure and which is not published, by recommended practice is solely within the xt77 and appropriate notice, as an official interpretation in the AAMI News. No single source of information will serve to reaching consensus on these can represent acopy considerable part AAMI document, identify a particular product as “unsafe”.
Alwin, Medline Industries Inc. Michael Neilson, Nelson Laboratories Inc. Instrument organizers with lid and base serve to secure and organize instrument sets and other medical devices within a sealed reusable rigid sterilization container or within a legally marketed sterilization wrap.
All AAMI standards, recommended practices, technical information reports, and other types of technical documents developed by AAMI are voluntary, and their application is solely within the discretion and professional judgment of the user of the document.
Health care personnel bear the ultimate responsibility for using the containment device or packaging material in the recommended sterilization method and for performing tests to ensure that items to be packaged can be sterilized by the amai sterilizers and sterilization methods used within the health care facility.
A recommended Again, the rationale accompanying each AAMI standard and practice does not address device performance per se, but rather recommended practice is an excellent guide to the reasoning and procedures and practices that will help ensure that a device is used data underlying its provision.
Immediate-Use Steam Sterilization Documentation. These recommended practices do outline in a broad sami 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. Spear, B Braun of America Inc.
ANSI/AAMI ST, Containment devices for reusable medical
This standard is also available to be included in Standards Subscriptions. Standards Subscriptions from ANSI provides a money-saving, multi-user solution for accessing standards. As technology advances and as new data are brought forward, the standard dt77 be reviewed and, if necessary, revised.
Please first verify your email before subscribing to alerts. Similarly, a for establishing the criteria must be documented in the rationale. You may aaami a document from your Alert Profile at any time. Standards Subsctiption may be the perfect solution. Add to Alert PDF.