Thompson
Fixed Wide Balfour [no lips] 100mm x 61mm (4" x 2 3⁄8")
Retractor Systems Instructions for Use
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Thompson Retractor
IMPORTANT INFORMATION FOR USE OF THOMPSON RETRACTOR SYSTEMS AND INSTRUMENT CASES
(NOT including illumination products, silicone sleeve, or discontinued Adjustable Height Rail Clamp. Please note, this does include the Infinite Height Rail Clamp.): This IFU is intended to assist health care personnel in safe handling practices, effective reprocessing, and maintenance of all Thompson Surgical Instruments, Inc.’s retractor systems and accessory families. End of usable life for metal surgical instruments is normally determined by wear and damage due to intended surgical use. All Thompson Retractor products and accessories are latex-free. EC
Thompson Surgical Instruments, Inc. 10341 East Cherry Bend Road Traverse City, Michigan 49684 *Indicate (RMA #) on return shipments*
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phone: fax:
(800) 227-7543 (IN USA) +1 (231) 922-0177 (OUTSIDE USA) +1 (231) 922-0174
0297
REP
Emergo Europe Prinsessegracht 20 2514 AP The Hague THE NETHERLANDS
IMPORTANT INFORMATION FOR USE OF THOMPSON RETRACTOR SYSTEMS AND INSTRUMENT CASES
ENGLISH PLEASE READ BEFORE USE
Failure to follow these instructions may render device unusable and may void warranty or service agreements. DESCRIPTION: The Thompson Retractor is a reusable device designed to provide access and exposure for a variety of surgical procedures. The Thompson Retractor is designed with interchangeable frame components, accessories, and blades to meet a variety of patient anatomies and procedures. SCOPE: This IFU provides recommended information for the cleaning and sterilization of reusable surgical retractor systems and accessories* that are manufactured and/or distributed by Thompson Surgical Instruments, Inc. Always reference our website, www.thompsonsurgical.com, for the most current revision of this IFU. *Accessories refer to our retractor system components such as adapters, wrenches, instrument cases, etc. This does NOT refer to our illumination products, silicone sleeve, or Adjustable Height Rail Clamp. INTENDED USE: The Thompson Retractor is intended for use during surgical procedures in order to provide surgical access and exposure. Thompson Surgical retractor systems and accessories are supplied non-sterile. This IFU is intended to assist health care personnel in safe use and handling practices, effective reprocessing, and maintenance of all Thompson Surgical Instruments, Inc.’s retractor systems and accessory families. All instruments must be inspected, cleaned, and sterilized prior to each use. CONTRAINDICATIONS: None known LIMITATIONS ON REPROCESSING: Repeat processing, according to the instructions in this IFU, has minimal effect on instrument life. Any limitations to reprocessing cycles will be noted in this IFU. WARNINGS AND PRECAUTIONS: PPE (Personal Protective Equipment): Should be worn, per individual hospital protocol, when handling or working with contaminated (or potentially contaminated) instruments. CJD (Creutzfeldt-Jakob Disease): Discard or destroy instruments in contact or exposed to patients with CJD, or those suspected of CJD. (Thompson Surgical does not advocate nor provide any validated instructions to eliminate risk of cross-contamination.) 1. Medical professionals should be familiar with all product support literature and videos to perform procedures with this device before use. 2. Many variables such as patient anatomy, pathology, and surgical techniques may influence the procedure’s outcome. Patient, product, and procedure selection is the responsibility of the medical professional. 3. Do not over-retract. Only use as much retraction as necessary to provide adequate exposure and access. 4. Relax the retractor periodically to ensure proper blood flow. 5. Avoid compressing the patient’s body with frame components to prevent nerve damage. See user manuals for proper setups and components to meet various patient anatomies. 6. Table mounted frame prevents most retractors from moving relative to patient movement. Use caution when moving patient while retractor is in use. 7. Do not move, retract, or adjust blades or frame components when blades are fixed to the spine with pins. 8. If using pins with blades, ensure pin distal end and thread is always engaged in spine to prevent unexpected sharps. Blade pins are not intended for distraction. 9. Products are provided non sterile and must be cleaned and sterilized before each use. 10. Normal repeated use has little effect on these instruments. Determine end of life by wear and damage due to use. 11. Product should be inspected before each use according to this IFU. Do not use products that show signs of damage such as cracking, deformation, or sharp edges. 12. Check stability of OR table rails or rail adapters/accessories before table mounting the Thompson Retractor. Only table mount to secure, non-movable rails and do not use if movement is evident. 13. Thompson Retractor products are only for use with other Thompson Retractor products unless otherwise specified by the manufacturer, such as through the offering of competitor adapter handles and other products. 14. Use of the Thompson Retractor for any purpose other than what is described here and in associated device user manuals, may cause damage or failure of the device which could result in serious patient injury or death. 15. US Federal Law restricts this device to sale to or on the order of a physician. 16. Retractor blades may compress nerves. User must evaluate the need to use free running EMG to monitor events such as retractor nerve compression outside of the visual field. DO’S AND DON’TS DO’S Use only soft, nylon brushes Use neutral (7) or low pH chemicals Use water-soluble instrument lube before each sterilization Pre-clean instruments before sterilizing Dry instruments prior to storing Protect instruments when storing Inspect instruments for damage Use distilled water when soaking instruments
DON’TS Use metal or abrasive brushes / pads Use high pH (>9) chemicals Use silicone lube or mineral oil Sterilize without first pre-cleaning Store instruments wet or semi-dry Store instruments unprotected / piled Use damaged / suspect instruments Use saline when soaking instruments
SYMBOL LEGEND: EC
Manufacturer
REP
EC Rep
0297 CE Mark
Warnings / Precautions
Biological Risks
DO NOT Reuse
Non-Sterile
Keep Dry / Protect from Moisture
DO NOT USE if Package Damaged / Compromised
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PROCESSING / REPROCESSING INSTRUCTIONS FOR THOMPSON RETRACTOR SYSTEMS AND INSTRUMENT CASES
(NOT including illumination products, silicone sleeve, or discontinued Adjustable Height Rail Clamp. Please note, this does include the Infinite Height Rail Clamp.): HOSPITAL MUST ENSURE OPERATIONS ARE PERFORMED USING THE APPROPRIATE EQUIPMENT, MATERIALS, AND TRAINED PERSONNEL. ANY DEVIATIONS FROM THIS IFU SHOULD BE EVALUATED FOR EFFECTIVENESS TO AVOID POTENTIAL ADVERSE CONSEQUENCES. CLEANING Adequate reprocessing is contingent upon the thoroughness of cleaning. To ensure acceptable reprocessing, do not delay between the steps below. Clean instruments as soon as reasonably practical, or within at least 30 minutes following use. Keep instruments moist and covered / wrapped until transported to Point of Use. DO NOT allow saline, blood, or other organic debris to dry on instruments. Point of Use / Pre-Cleaning Instructions: 1. Disassemble, loosen, or unlock instruments where possible, without the use of tools (ex: screwdriver.) 2. Rinse/flush instruments under cool or lukewarm running water. 3. Remove excess soil while rinsing, using non-abrasive brush/cloth. NOTE: Do not completely submerge Articulating Arm central black knob during cleaning. Ensure knob is tightened during cleaning but open during sterilization. Manual Cleaning is NOT ALLOWED for Articulating Arm. Manual Cleaning: Automated Cleaning: 1. Soak instruments in prepared enzymatic solution for 20 minutes, as shown below in Table A. 1. Rinse instruments with cold tap water for 2 minutes, ensure visible contamination is removed. 2. Gently scrub all surfaces, including crevices and hard-to-reach areas, with soft, nylon brush. 2. Scrub instruments with soft brush, as necessary. 3. Remove / rinse instruments under water for 3 minutes-thoroughly and aggressively flush 3. Load instruments into automated washer/disinfector in fully extended, open positions to difficult to reach areas. maximize surface exposure. 4. Submerge instruments in prepared detergent of ultrasonic unit for 10 minutes at 45-50 kHz. 4. Run washer according to Thompson’s validated cleaning cycle shown below in Table B. 5. Rinse instruments in purified / distilled water for 3 minutes, or until no visible contamination remains. 5. Check instruments for visible contamination following automated cycle. If soil is present, repeat 6. Repeat above sonication and rinse steps. the cleaning process. Do not proceed with reprocessing of a soiled instrument. 7. Dry instruments using clean, lint-free cloth and/or compressed air to remove moisture from crevices and hard to reach areas. 8. Repeat if necessary.
Table A: Manual Cleaning Cleaning Agents Used in Manual Cleaning Validation (prepared according to Manufacturer’s recommendations): · Enzol® by Johnson & Johnson (1 oz/gal, using lukewarm tap water) · ValSure® Neutral Detergent by Steris (1/4 oz/gal, using lukewarm tap water in ultrasonic unit) Final Rinse Used in Manual Cleaning Validation: Reverse Osmosis / Deionized water (RO/DI)
PHASE Pre-Wash Enzyme Wash Wash 1 Rinse 1 PURW Rinse Drying
Table B: Automated Cleaning TIME (MIN.) TEMP. DETERGENT/ CONCENTRATION 02:00 Cold Tap Water N/A 01:00 Hot Tap Water Enzol® by J&J (1 oz/gal) 02:00 66ºC (151ºF) (set point) Renu-Klenz™ by Steris (1/4 oz/gal) 00:15 Hot Tap Water N/A 00:10 (non-recirculation) 66ºC (151ºF) N/A 07:00 115.5ºC (240ºF) N/A
STERILIZATION 1. Prepare instruments for sterilization by loosening, unlocking, and disassembling all moving mechanisms or removable parts where possible without the use of tools. NOTE: All Elite Rail Clamps may be sterilized with the top tightening knob and jaw in any position. 2. Arrange instruments in dedicated instrument trays to ensure sterilization can penetrate all surfaces. 3. Wrap instruments or instrument tray in 2 layers of 1-ply polypropylene wrap, using sequential wrapping techniques. 4. Place wrapped instruments in sterilizer, following validated parameters as indicated below. Prevacuum Steam Sterilization Parameters Validated Gravity Steam Sterilization Parameters Validated Sterilizer Type: Prevacuum Sterilizer Type: Gravity Preconditioning Pulses: 4 Temperature: 121ºC (250ºF) Temperature: 132ºC (270ºF) Exposure Time: 30 Minutes Exposure Time: 4 Minutes Dry Time: 30 Minutes* Dry Time: 30 Minutes* *The dry times were validated utilizing a 15 minute open door phase and 30 minute cool down phase. Total weight of wrapped instruments or tray may not exceed PRODUCT METHOD CYCLE CYCLE TEMP EXPOSURE TIME MIN. DRY TIME CYCLES 11.4kg (25 pounds). Weight gain, post-sterilization must not Thompson Retractor Steam Prevacuum 132ºC (270ºF) 4 Minutes 30 Minutes Unlimited exceed 3% of 11.4kg (25 pounds). Thompson Retractor Steam Gravity 121ºC (250ºF) 30 Minutes 30 Minutes Unlimited INSPECTION, LUBRICATION, AND TESTING 1. Carefully inspect instruments to ensure all visible contamination removed. Reassemble instruments, as necessary, to test instrument function. 2. Lubricate all moving mechanisms on instruments with a steam penetrable, water-soluble product after every cleaning cycle. (Such as Surgislip® by Ruhof.) 3. Test action of movable parts to ensure smooth operation / uninhibited movement. · Do not use any instruments that appear damaged or broken (cracked, deformed, nonfunctional, or altered). · Lubricate articulated instruments after every cleaning cycle. STORAGE AND USE If package integrity is compromised or suspect, repeat Processing / Reprocessing Instructions. STORAGE: Store sterile, packaged instruments in a limited access area that is well-ventilated, protected from contaminants, and dry. USE: Carefully examine sterile instrument packaging prior to use, ensuring package integrity is maintained. EQUIPMENT RETURNS: HOSPITAL RESPONSIBILITIES ALL loaner and trial equipment returns must be fully reprocessed before shipping to Thompson Surgical Instruments, Inc. (10341 East Cherry Bend Road, Traverse City, MI 49684). Hospital must indicate cleaning / sterilization of instruments on return packaging. RMA must be referenced on outside of package. Prevent damage of returned equipment: · ALWAYS place parts in designated holders / spaces when using organized instrument cases. · NEVER ship Elite II Rail Clamps / Infinite Height Rail Clamps / Power Rail Clamps inside instrument cases; MUST package separately. PRODUCT WARRANTY Thompson Surgical Instruments, Inc. warrants all instruments free from defects in material or workmanship for 10 years*. Warranty void if product failure resulted from normal wear and tear from instrument use, accident, abuse, misapplication, negligence, or if the product has been damaged, altered, or repaired outside of Thompson Surgical’s facility. Warranty void if purchased from a non-authorized supplier/distributor. Note that aluminum blades are sensitive to high and low pH levels. Please follow cleaning and sterilization instructions exactly. Failure to do so may cause aluminum blade staining, pitting, or other corrosion and will void blade warranty. * Malleable and Cobra blades carry a 2 year guarantee against defects in both material and workmanship. Blade finishes do not carry a warranty. Please replace Cobra blades after 2 years of surgical use or 200 uses if this occurs first to avoid possible fracturing or cracking of Cobra blade tips. Hip Tethers carry a 1 year guarantee against defects in both material and workmanship. Please replace Hip Tethers after 10 reprocessing cycles to avoid possible breakage. (Illumination Products: Xenon products carry a 60 day guarantee; LED products carry a 1 year guarantee.) REFURBISHMENT PROGRAM AND POLICY Your Thompson Retractor may be sent in and refurbished back to like-new quality. Free loaner sets are available while your equipment is being refurbished. Some limitations apply. Any refurbishments made outside of our facility will void the warranty. Please contact your Account Manager at 1-800-227-7543, or visit our website www.thompsonsurgical.com for details.
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