Cleaning Validation

Disinfect Med Devices Pt. 3

How to Properly Disinfect Reusable Medical Devices: Part III In Part II of “How to Properly Disinfect Reusable Medical Devices” (Novo blog 12/1/17) we discussed various disinfectants that are commercially...
December 8, 2017
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Disinfect Med. Devices: Pt. 2

In Part I of “How to Properly Disinfect Reusable Medical Devices” (Novo blog 11/24/17) disinfection was defined as “The process designed to eliminate all pathogenic microorganisms, except bacterial spores, from...
November 30, 2017
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Instrument Checklist Part II

A Checklist For Purchasing New Surgical Instruments: Part II The first step in reducing your patients’ risk of a surgical site infection (SSI) caused by a contaminated surgical instrument begins...
October 20, 2017
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Storing Sterile Instruments

How To Store Sterilized Surgical Instruments The proper storage of sterilized instruments is extremely important in order to protect them from contamination prior to their use in surgery on patients....
September 14, 2017
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The Cost of SSIs

The Costs Associated with a Surgical Infection & Validated IFUs According to the Centers for Disease Control and Prevention (CDC), surgical site infections (SSIs) cost U.S. hospitals well in excess...
September 4, 2017
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Preventing HAIs

The Importance of Validated IFUs in Preventing Reusable Device Related HAIs According to the Centers for Disease Control, hospital acquired infections (HAIs) are one of the leading causes of morbidity...
August 18, 2017
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Validated IFUs & Sepsis

Can Validated IFUs Help In The Fight Against Sepsis? Sepsis is a leading cause of death in U.S. hospitals, according to the Sepsis Alliance, a nationwide advocacy group committed to...
August 10, 2017
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A Little Background on IFUs

These are disassembled Kerrison Rongeurs that were reprocessed using the manufacturer’s non-validated IFUs. (And Why They Are So Important) The FDA mandates that all reusable medical device manufacturers provide instructions...
August 4, 2017
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Duodenoscope Recall & Validated IFUs

FDA Safety Communication: Duodenoscope Recall by Fujifilm © On July 21, 2017, Fujifilm© issued an Urgent Medical Device Correction and Removal notification informing customers of its voluntary recall of all...
July 30, 2017
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Definition of an IFU & Its Impact on Patient Safety

Complying with manufacturer’s instructions for use (IFUs) is an important patient safety issue. As too many recent headlines have shown, failure to comply with IFUs can result in a contaminated...
July 20, 2017
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