Declaration of Classification ValiSpore Incubator Manual

Similar documents
EZTest Incubator OPERATION MANUAL. 10 Evergreen Drive Bozeman, MT USA (303) Model

1510 Self-Contained Biological Indicator Incubator OPERATION MANUAL

Operating Manual for HEKA Incubators

Setting a new standard for performance, safety and simplicity

Isolette TI500 Neonatal Transport

Personal Health Monitoring Services SM VITAL SIGNS TRANSMITTER MODEL: VST 3 TM. Instruction Manual

Key to BEDSIDE External Pulse Generator Controls and Features

Medical Grade Power Strips

CMS REQUIREMENTS: ESSENTIAL ELEMENTS FOR ASCS

Product Introduction. Specification Sheet. Certificates. Application. Features. Street Light

Specifications, Performance & Submittal

smart technologies Neonatal incubator from standard to intensive care

3M Sterilization Assurance Standards Practice. In Sterilization with the Core Four

Medical furniture OPTIMA OBSTETRIC BED

TESTING APPLICATION STANDARD (TAS) IMPACT TEST PROCEDURES

smart technologies Neonatal incubator from standard to intensive care

Carter Healthcare, Inc

Siemens TEC Unit Vent 0-10V Output Controller. Accessories. Control Applications. Product Description. Product Numbers. Warning/Caution Notation

Compounded Sterile Preparations Pharmacy Content Outline May 2018

Image 3. exclusive design to meet all your needs

Position within the Organisation GP Research Lead

Lodestar. Series. Specification Sheet. Application. Features. Floodlight. Tunnel Lighting. Parking Applications. Canopy Lighting Wash Lighting.

Audio. Distribution. Network ADN C1/ADN D1. Quick guide

DEPARTMENT OF THE ARMY SUPPLY BULLETIN

Approved for public release. Distribution is unlimited.

Oak Grove School District Respiratory Protection Program

Efficient Use of Valuable Space

Administrative Policies and Procedures. Policy No.: N/A Title: Medical Equipment Management Plan

REVEAL. Patient Assistant 9538/9539. Clinician Manual. Caution: Federal Law (USA) restricts this device to sale by or on the order of a physician.

NJ Dept of Health Central Service Standards SUBCHAPTER 8. CENTRAL SERVICE. 8:43G-8.1 Central service policies and procedures

TECHNICAL MANUAL OPERATOR'S, UNIT, DIRECT SUPPORT, AND GENERAL SUPPORT MAINTENANCE MANUAL

STATE OF OHIO DEPARTMENT OF TRANSPORTATION SUPPLEMENT 1041 ASPHALT CONCRETE QUALITY ASSURANCE PROGRAM ADMINISTRATION.

RESPIRATORY PROTECTION PROGRAM

ENTERPRISE with people in mind

Smoke Control BACnet PTEC Unit Vent Controller. Control Applications. Product Description. Product Numbers

OSHA Preparedness. Presented by: Dave Lall, CEO, DEMILEC (USA) LLC

Caution! triangles are used to warn of situations that demand extra care and attention.

Organization for Economic Co-operation and Development

Sterile Compounding of Hazardous Drugs

Eleganza 3XC. Designed for ICU

EasyCare Maximizing Care, Comfort and Safety

Standard EC Elements of Performance for EC The hospital manages fire risks.

Pharmacy General Personnel

Best Practices for MANAGING MEDICAL EQUIPMENT AND SUPPLIES

User Manual for Spirit Beds

Laboratory Accreditation Program CRITERIA

Australian/New Zealand Standard

Isolette 8000 Neonatal Closed Care

Summary Report for Individual Task TROUBLESHOOT THE AVIATION GROUND POWER UNIT (AGPU) Status: Approved

Laboratory Risk Assessment: IQCP and Beyond. Ron S. Quicho, MS Associate Project Director Standards and Survey Methods, Laboratory July 18, 2017

MAXI SKY 2 THE NEXT GENERATION CEILING LIFT SOLUTION

Feel at home. No matter where you stay. TECHNICAL MANUAL

MONITORING. learning objectives:

9/14/2017. Best Practices in Instrument Cleaning. Objectives. Healthcare-associated Infections

SOP WP6-QUAL-04, Version 1.0, 23 February 2014 Page 1 of 8. SOP Title: Laboratory (GCLP) supervision visits

Simply Intuitive. The Hill-Rom Advanta 2 Bed

SARASOTA MEMORIAL HOSPITAL

Pressure IQ Evolve Mattress Replacement System USER MANUAL

250- PERSONAL PROTECTIVE EQUIPMENT PROGRAM

Intravenous Medication Administration via a Central Venous Line

Summary Report for Individual Task E-1102 Repair Communications System Control C-6533(*)/ARC Status: Approved

FlexoStretch. Product Description. Instruction Guide

COMMERCIAL ITEM DESCRIPTION SPECIFICATION SHEET CIRCUIT BREAKER, 28 VOLTS (V) DC, AUTOMATIC RESET, NONWATERPROOF, 10 AMPERES (A) TO 35 A

Incident Reporting, Notification, and Review Procedure

C. Physician s orders for medication, treatment, care and diet shall be reviewed and reordered no less frequently than every two (2) months.

Section 5 General Policies Work, Health and Safety Policy. The Gums Childcare Centre Policies

REQUEST FOR PROPOSALS

SURGICAL SERVICE SPECIALTY. Set Up and Safe Operation of Equipment

PHARMACY SERVICES / MEDICATION USE

3.03 Functions of support services personnel Name

Summary Report for Individual Task E-1069 Maintain the KVG-72(*) Status: Approved

Redefining Patient Handling. prevention

USP 797: A FOCUS ON ANTIMICROBIAL RISK LEVEL KAREN MILKIEWICZ, PHARMD

NRC INSPECTION MANUAL

Summary of Learning Outcomes Level 3 Award in Supervising Food Safety in Catering Qualification Number: 500/5471/5

Instruction for use and trouble shooting guide

BioZone Protectant Antimicrobial Coating

1 What is an AAAHC/Medicare Deemed Status survey? 2 What are the Medicare Conditions for Coverage (CfC)?

EQUIPMENT MANAGEMENT MEDICAL EQUIPMENT: EC , EC UTILITY SYSTEMS: EC , EC

Redefining Patient Handling. prevention

Instant results with a simple touch

To provide information about the role of the pharmacy in Infection Prevention and Control.

Technical Supplement For Joint Standard Instrumentation Suite Missile Attitude Subsystem (JMAS) Version 1.0

1.2 billion ambulatory care visits in US: physician offices, outpatient hospital and ED

INDIAN ASSOCIATION FOR THE CULTIVATION OF SCIENCE 2A & 2B Raja S.C.Mullick Road Jadavpur, Kolkata

To provide protocol for medication and solution labeling to ensure safe medication administration. Unofficial Copy

KPIC Aseptic Technique Training Program

Facility Standards. 10/23/2013 Facility Standards for San Juan College Veterinary Technology Program OCCI Sites Page 1 of 5

KPIC Aseptic Technique Training Program Friday, August 24 th Saturday, August 25 th, 2018

MCC. SMBJP6KE6.8(C)A THRU SMBJP6KE550(C)A. Features. Transient Voltage Suppressor 6.8 to 550 Volts 600 Watt.

LESSON ASSIGNMENT. After completing this lesson, you should be able to: 2-3. Distinguish between medical and surgical aseptic technique.

Observations will be made of the storage. knowledge of the hazardous materials. labeling the container to the use of. containers (which may range from

STANDARDS Point-of-Care Testing

PROCESS IMPROVEMENT AND ENHANCED QUALITY CARE ARE THE

Instructions for use. Unfold and lay flat. Read both sides for full instructions

2016 Sterilization Standards Update

Isolette 8000 plus Neonatal Closed Care

Administration of IV Medication in the Community by the Children s Community Nursing Team Standard Operating Procedure

Best Practices for Equipment Calibration and Analytical Controls in the Diagnostics Laboratory

Buck & Boost Transformer Installation Instructions

Transcription:

alisafe Declaration of Classification ValiSpore Incubator Manual I hereby confirm that the Valisafe chemical indicators used to monitor steam sterilization are an accessory to a class 1 medical device and therefore are not categorized as class 1 medical device. Yours Sincerely, Lawrence Dawson CEO Valisafe Twyford Road Bishop s Stortford Hertfordshire CM23 3LJ T: +44 (0)1279 461641 F: +44 (0)1279 461643 www.valisafe.com E:info@valisafe.com 1 Valisafe is a division of Medisafe International www.medisafeinternational.com

Contents Safety Information 03 Specifications 04 Installation & Warm up 05 Temperature Selection 06 Operation 07-08 Maintenance 09 Cert Conformity 10 Introduction The Valisafe biological indicator incubator is designed for convenient and effective incubation of self-contained biological indicators requiring incubation temperatures of 37 C, 57 C, or 60 C. The incubator features a built-in thermometer with LED display, 13 incubation cavities, and an integrated activation (crushing) cavity. A self-contained biological indicator consists of a capped thermoplastic culturing vial containing a glass media ampoule and a carrier inoculated with bacterial spores. Upon removal from the sterilizer, the indicator is activated by flexing the plastic culturing vial to crush the inner glass ampoule which allows the growth medium to contact the spore carrier. The activated indicator is then incubated for a specified length of time and observed for colour change of the growth medium. If the medium turns yellow during incubation, the test is positive indicating growth and inadequate sterilization. 2

Safety Information Handle with caution. The surface of the incubator may become hot to the touch. The incubator has been designed with function, reliability, and safety in mind. It is the user s responsibility to install it in conformance with local electrical codes. For safe operation, please pay attention to the alert boxes throughout the manual.! Refer to manual. Cautions alert you to potential equipment damage and hazards. Notes alert you to pertinent facts and conditions. Use only as directed Indoor use only. Temperature 10 C to 35 C. Maximum relative humidity 80% for temperatures up to 31 C decreasing linearly to 50% relative humidity at 35 C. Main power supply voltage fluctuations not to exceed ±10% of the nominal voltage. Installation class II service. Polution-Degree 2 environments. Altitude less than 2000m. 3

Specifications Incubator specifications Overall Dimensions Width 3.5 in / 9 cm Height Depth Weight Incubation Cavities Number 13 Diameter Depth 2.0 in / 5.08 cm 4.0 in / 10.2 cm 0.89 lb / 0.4 kg 0.375 in / 0.94 cm 1 in / 2.54 cm Thermometer Accuracy +/- 1 C Electrical Ratings (for use with certified class 2 power supply) Volts I1410 12VDC Watts 18.0 Amps 1500 ma Operating Range Temperature 37 C / 57 C / 60 C Environmental Conditions Ambient Temperature 10 C - 35 C Relative Humidity 20% - 80% Non-condensing Conformance CSA/C/US, CE, RoHS, FCC Part 15 Class A, ICES-003 Class A Power Supply P6-1000 Rated Input Voltage 100-240VAC Input Voltage Range 90-264VAC Rated Frequency 50-60Hz Rated Input Current 1.0A Output Voltage 12VDC Max Output Current 2.5A Max Output Wattage 30W Saftey Approvals UL/cUL, GS, CCC, RCM EMC / EMI FCC class B, CE, VCC I class II RoHS Compliant Yes Storage Temperature -10 C - 70 C Storage Humidity 10-90% Operating Temperature 0-40 C Operating Relative Humidity 20 80% 4

Installation and Warm Up The incubator is designed for continuous operation and does not have a power switch. The incubator will power on when it is plugged into a power source. Note: the incubator must be installed in a location where temperature is maintained between 10 C (50 F) and 35 C (95 F). 1. Remove the incubator from its packaging. 2. Unpack the power supply. The power supply includes four interchangeable blades (plugs). Select the appropriate blades (plugs) for your region and attach the blades to the power supply. 3. Plug the power supply into a power source. 4. Insert the small connector from the power supply into the matching receptical in the back of the incubator (see Figure 1). 5. The incubator will automatically power on and perform a self-test. Upon completion, the installed firmware revision will be displayed on the LED screen for two seconds. 6. The incubator will begin its warm-up phase. During this time the configured temperature setpoint will fade in and out on the LED screen. 7. The incubator is ready to use when the configured setpoint is no longer fading in and out, and the LED screen displays the current operating temperature of the incubator. Note: it may take approximately 15 minutes for the incubator to warm up to operating temperature, depending on the selected incubation temperature and the temperature of the environment in which the incubator is installed. 5

Temperature Selection The incubator can be configured to operate at 37 C for biological indicators containing Bacillus atrophaeus, or 57 C or 60 C for biological indicators containing Geobacillus stearothermophilus. The incubator is initially configured to operate at 60 C. Caution: failure to set the correct incubation temperature will yield invalid test results. It is not possible to incubate at multiple temperatures simultaneously. Refer to the instructions for use for your biological indicators to select the appropriate incubation temperature. 1.With the incubator powered on, simultaneously press and hold the two small buttons on the rear of the incubator (see Figure 1) for ~2 seconds until the currently selected temperature setpoint blinks on the LED display. 2. Release the buttons, then press either button repeatedly to toggle between the available temperature setpoints (37 C, 57 C, or 60 C). 3. When the desired temperature setpoint is blinking on the display, press and hold both buttons for ~2 seconds. 4. The configured setpoint will fade in and out on the LED screen until the incubator has reached temperature, upon which the actual temperature of the incubator will be displayed. Figure 1 - Rear of Incubator 6

Operation Note: refer to the instructions for use supplied with your biological indicators for information on processing, incubation, interpretation of results, and using positive controls. When the incubator has reached the configured temperature, the actual temperature of the incubator will be shown on the LED display, indicating that the unit is ready to accept biological indicators. Verify that the temperature displayed is within the allowable range for your biological indicator before proceeding (see the instructions for use supplied with your biological indicators). Biological Indicator Activation Prior to incubation, the biological indicator must be activated by crushing its internal glass medium ampoule. This allows the color-change medium from the ampoule to contact the spore carrier.! WARNING: allow a processed BI to cool for at least 10 minutes upon removal from the sterilizer. Failure to do so may cause the glass medium ampoule to burst during activation, resulting in injury from hot liquid or flying debris. The incubator contains an activation (crushing) cavity to simplify activation (see Figure 2). Place the processed or positive control biological indicator into the left side of the activation cavity and flex the indicator to the right until the glass ampoule breaks. Note: you may have to grip the incubator by the base while activating a BI so that it does not tip over. 7

Operation Incubation To confirm adequate sterilization (negative result), self-contained biological indicators must be incubated for the appropriate length of time ( incubation time ). Please refer to the instructions for use that came with your biological indicators for the proper incubation time. Immediately upon activation, place the indicator into one of the thirteen numbered incubation cavities (see Figure 2). Record the incubation start time and cavity number. Observe the color of the growth medium in the BI at regular intervals during incubation. A color change to yellow during the incubation time indicates bacterial growth (positive test). If the incubation time expires and no color change to yellow is observed, this indicates a negative test. Caution: if a positive control does not grow, do not use the remaining units from the box and contact your dealer immediately. A positive control that does not turn yellow is a serious problem. Fortunately, the causes are few: a grossly malfunctioning incubator, inadvertent sterilization of the control vial, inadvertent sterilization of the box of indicators, or improper storage. If the control is negative because of one of the latter two causes, do not use any of the other biological indicators from the same box. Dispose of positive or negative BIs immediately per the instructions for use that accompany each box of indicators, or per your organization s policy. Figure 2 Top of Incubator 8

Maintenance The incubator requires no maintenance other than cleaning as necessary. Cleaning 1. Unplug the incubator before cleaning. 2. To clean the exterior, use a cloth dampened with isopropyl alcohol. 3. To clean the incubation and activation cavities, use a cotton swab dampened with isopropyl alcohol.! WARNING: DO NOT IMMERSE THE UNIT IN ANY LIQUID AND DO NOT SPRAY OR POUR LIQUID DIRECTLY ONTO THE UNIT. Temperature Verification The incubator, including the LED temperature display, is factory calibrated using a NIST traceable temperature standard and does not require user calibration. Incubation temperature can be verified by placing an NIST traceable thermometer into one of the incubation cavities and allowing 30 minutes for temperature stabilization. The temperature reading should be within +/- 2 C of the incubator set-point temperature. 9

Certificate of Conformity Date of issue: June 2010 Product Number: Product Description: Unit: CE marked Standards to which this product conforms to: Shelf life: V3504035 ValiSpore Incubator 1 x 14 cavity incubator Yes N/A Extended Life Valisafe is a division of Medisafe UK Ltd. Valisafe Twyford Road Bishop s Stortford Hertfordshire CM23 3LJ UK T: +44 (0)1279 461641 F: +44 (0)1279 461643 www.valisafe.com E:info@valisafe.com Valisafe is a division of Medisafe International www.medisafeinternational.com 10

ValiSpore Steam 10x5 ValiSpore Steam 10x6 ValiSpore EO 10x6 alisafe clearly a better indicator Conforms to ISO 11138 Contains Geobacillus Stearothermophilus for Steam sterilization and Bacillus Atrophaeus for Ethylene Oxide Sterilisation Easy to incubate no laboratory conditions for culturing Dramatic colour change for positive cultures Results in 24 hours for steam and 48 hours for Ethylene Oxide Easy to use Non-hazardous according to EC Regulation 1907/2006 ValiSpore Steam 10x5, ValiSpore Steam 10x6, ValiSpore EO 10x6 Valispore biological indicators for Steam and Ethylene Oxide contain a known quantity of bacterial spores inoculated onto filter paper placed inside a plastic culture with a crushable glass ampoule containing the culture medium ( traceable to a recognizable culture identified in USP and ISO 11138). Valispore Biological indicators are certified for population, D-value, Z-value and performance. They are manufactured in compliance to USP and ISO 11138. Order Details V3504000 ValiSpore 10x5 box 100 units V3504005 ValiSpore 10x6 box 100 units V3504010 ValiSpore EO 10x6 box 100 units V3504035 ValiSpore Incubator 1 unit 11 Ref: Valisafe Tech Sheets 07/10 Rev.C