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The Journal of the ISRP has been published regularly since 1984, and is published twice a year. Since 2002, the journal has also been published on-line, along with the printed version. To date, almost 100 issues of the journal have been compiled, printed and distributed to members. This means hundreds of research papers and articles over some 4,500 reprocessing, and sterilization. Not only does the FDA approve medical devices, but FDA inspectors also examines medical devices at their manufacturing facilities. Many quality problems that the FDA identifies have to do with manufacturing failuresrelated to either biocompatibility, reprocessing, or sterilization.
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This study defines reprocessing protocols and evaluates their effectiveness against a pandemic influenza strain in a laboratory setting. Methods: Five half-mask elastomeric respirator models and 3 powered air-purifying respirator models were contaminated with influenza virus and artificial skin oil on multiple surfaces. Appendix B-2 to § 1910.134: Respirator Cleaning Procedures (Mandatory) These procedures are provided for employer use when cleaning respirators. They are general in nature, and the employer as an alternative may use the cleaning recommendations provided by the manufacturer of the respirators used by their employees, provided such procedures are as effective as those listed here in Appendix B- 2. allocation of N95 respirators and surgical/procedure masks based on exposure risk 3.
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Fit testing may be required. Fit checking is always required. 3. Manual reprocessing for reusable respirators were evaluated against influenza and soiling agent.
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