#Stryker system 6 instructions install
#Stryker system 6 instructions code
#Stryker system 6 instructions series

The minimum recommended Washer/Disinfector cycle is below:.

DO NOT overload the trays.Д«) Arrange medical devices so that cannulations are not horizontal and battery openings are oriented downwards (to assist drainage).

Load the medical devices into the Washer Disinfector.ДЄ) Avoid contact between devices (movement during washing could cause damage and washing action could be obstructed).

Determination of cleaning agents shall be by local or country regulations. Prepare mild pH enzyme and cleaning agents at the use-dilution and temperature recommended by the manufacturer. This can be accomplished by holding the hose end over end to allow all liquid to drain. If pneumatic hose is used in lieu of a washer cap, the hose must be drained of all residual fluids prior to sterilization.

#Stryker system 6 instructions install

For Manual Cleaning install the Washer Cap (as defined above) or the appropriate pneumatic hose or electric cable for the instrument.3M Maxi Style Hose Connector вЂ“ CAP-300MAX.MicroAire Style Hose Connector вЂ“ CAP-100.For Automated Cleaning install the Washer Cap for the instruments listed.Disassemble instruments and accessories.Reuse of surgical cutting accessories is not recommended. Disposable surgical accessories should be discarded after use, handling them as any contaminated sharp accessory is handled. Remove all inserted surgical cutting accessories (blades, burs, rasps, drill bits, etc.) from the handpiece.Body fluids and tissue should not be allowed to dry on instruments prior to cleaning (MAXIMUM 30 minutes). Remove excess body fluids and tissue with a disposable, non-shedding wipe and cover with a cloth dampened with purified water. End of life is normally determined by wear and damage due to use. Repeated processing, according to the instructions below, has minimal effect on MicroAire reusable surgical instruments. DO NOT utilize cleaning agents with chlorine or chloride as the active ingredient is corrosive to stainless steel.DO NOT utilize cleaning solutions that are not mild pH unless they are approved for use with Anodized Aluminum and Surgical Instruments.DO NOT immerse the handpiece in any fluid.Also take special precautions to avoid the use of cleaners that contain lubrication. Lubrication may damage the internal motor mechanism. DO NOT lubricate or oil the handpieces.Universal precautions for handling contaminated materials should be observed at all times.Power Assisted Lipoplasty Electric and Pneumatic Instrument Д¬arpal Tunnel Release System (CTRS) Warnings:

#Stryker system 6 instructions series

SmartDriver Electric, Battery and Pneumatic Instrument and Couplers Д§000 Series Electric, Battery and Pneumatic Instruments and Couplers,

#Stryker system 6 instructions code

Learn more about medical device recalls.Дў Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.ДЈ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 В§7.55.ДҐ10(K)s with Product Code = KIJ and Original Applicant = STRYKER CORP.Per ISO 17664:2003 & AAMI ST 81:2004 Device(s):ДЎ000 & 2000 Series Electric and Pneumatic Motors and Couplers ДҐ000 Series Electric Motors and Couplers, The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Worldwide Distribution including USA and countries of Australia, Brazil, Canada, Chile, Colombia, Costa Rica, England, France, Germany, Greece, Hong Kong, India, Ireland, Israel, Italy, Japan, Malaysia, Netherlands, New Zealand, Pakistan, Panama, Peru, Philippines, Poland, Romania, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan and Turkey.ДЎ A record in this database is created when a firm initiates a correction or removal action. Consignees were also instructed on the following: 1) Review the letter and distribute to all affected departments, 2) Complete and sign the enclosed Business Reply Form and fax to 33 and 3) Call Stryker Instruments Service Department at 88 to schedule service for the handpieces. The handpieces may continue to run even when the trigger is not depressed, which could result in the unintended cutting of bone or soft tissue damage.Д¬onsignees were notified of the problem via letter dated October 10, 2008, provided interim instructions to reduce the risk, and informed that Stryker instruments will replace the trigger on all handpieces. The product is an oscillating cutting device used for cutting bone and bone related tissue. Note: The product label declares the product to be a handpiece. Stryker Instruments, Kalamazoo, MI REF 6208. Stryker Sagittal Saw, For use with Stryker System 6. Instrument, surgical, orthopedic, dc-powered motor and accessory/attachment - Product Code KIJ Class 2 Device Recall Stryker System 6 Sagittal Saw